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8528 (T > C)

General info

Mitimpact ID
MI.1789
Chr
chrM
Start
8528
Ref
T
Alt
C
Gene symbol
MT-ATP8 Extended gene annotation
Gene position
163
Gene start
8366
Gene end
8572
Gene strand
+
Codon substitution
TGA/CGA
AA pos
55
AA ref
W
AA alt
R
Functional effect
missense
OMIM ID
516070
HGVS
NC_012920.1:g.8528T>C
HGNC ID
7415
RC complex
V
Ensembl gene ID
ENSG00000228253
Ensembl protein ID
ENSP00000355265
Ensembl transcript ID
ENST00000361851
Uniprot ID
P03928
Uniprot name
ATP8_HUMAN
Ncbi gene ID
4509
Ncbi protein ID
YP_003024030.1
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Powered by MitoWheel

Conservation

PhyloP 100v
7.698 Conservation Score
PhyloP 470way
0.742 Conservation Score
PhastCons 100v
1 Conservation Score
PhastCons 470way
0.965 Conservation Score

Pathogenicity predictors

PolyPhen2
Probably damaging Score and details of the predictor
SIFT
Neutral Score and details of the predictor
SIFT4G
Damaging Score and details of the predictor
VEST
Neutral Score and details of the predictor
MitoClass 1
Damaging Score and details of the predictor
SNPDryad
Pathogenic Score and details of the predictor
MutationTaster
.
fathmm
.
AlphaMissense
Likely pathogenic Score and details of the predictor
CADD
Deleterious Score and details of the predictor
PROVEAN
Damaging Score and details of the predictor
Mutation Assessor
.
EFIN SP
Neutral Score and details of the predictor
EFIN HD
Damaging Score and details of the predictor
MLC
Deleterious Score and details of the predictor
PANTHER
.
PhD-SNP
.

Pathogenicity meta-predictors

APOGEE1
Pathogenic Score and details of the meta-predictor
APOGEE2
Likely-pathogenic Score and details of the meta-predictor
CAROL
Deleterious Score and details of the meta-predictor
Condel
Neutral Score and details of the meta-predictor
COVEC WMV
Deleterious Score and details of the meta-predictor
MtoolBox
Deleterious Score and details of the meta-predictor
DEOGEN2
.
Meta SNP
.

Cancer-specific predictors

PolyPhen2 transf
Low impact Score and details of the cancer-specific predictor
SIFT transf
Medium impact Score and details of the cancer-specific predictor
MutationAssessor transf
High impact Score and details of the cancer-specific predictor
CHASM
Neutral Score and details of the cancer-specific predictor

Databases of Frequencies and Phenotypes

Clinvar ID
9640
Clinvar ALLELEID
24679
Clinvar CLNDISDB
Mondo:mondo:0044970, medgen:c0751651, orphanet:68380;

human phenotype ontology:hp:0005152, mondo:mondo:0010771, medgen:c1708371, omim:500000, orphanet:137675;

mondo:mondo:0010777, medgen:c2748884, omim:500006
Clinvar CLNDN
Mitochondrial disease;

histiocytoid cardiomyopathy;

cardiomyopathy, infantile hypertrophic
Clinvar CLNSIG
Likely pathogenic
MITOMAP Allele
8528T>C
MITOMAP Disease Clinical info
Infantile cardiomyopathy / hyperammonemia
MITOMAP Disease Status
Cfrm [lp]
MITOMAP Disease Hom/Het
+/+
MITOMAP General GenBank Freq
0.0%
MITOMAP General GenBank Seqs
0
MITOMAP General GenBank Curated refs
26803244 30642647 19188198 27409572 26741492 34298071 33180048 30763462 21457906
MITOMAP Variant Class
disease
Gnomad AN
0
Gnomad AC hom
0
Gnomad AF hom
0.0
Gnomad AC het
.
Gnomad AF het
.
Gnomad filter
.
HelixMTdb AC hom
0
HelixMTdb AF hom
0.0
HelixMTdb AC het
.
HelixMTdb AF het
0.0
HelixMTdb mean ARF
0.0
HelixMTdb max ARF
.
ToMMo JPN54K AC
.
ToMMo JPN54K AF
.
ToMMo JPN54K AN
.
COSMIC 90
.
dbSNP 156
.

Residue interaction

EVmutation
Site A-B InterP
Site A-B IntraP
ΔΔG intra
ΔΔG intra interface
ΔΔG inter

Compensated Pathogenic Deviations

Frequency
.
AA ref
.
CPD AA alt
.
Aln pos
.
RefSeq protein ID
.
Species name
.
Ncbi taxon ID
.

8528 (T > G)

General info

Mitimpact ID
MI.1788
Chr
chrM
Start
8528
Ref
T
Alt
G
Gene symbol
MT-ATP8 Extended gene annotation
Gene position
163
Gene start
8366
Gene end
8572
Gene strand
+
Codon substitution
TGA/GGA
AA pos
55
AA ref
W
AA alt
G
Functional effect
missense
OMIM ID
516070
HGVS
NC_012920.1:g.8528T>G
HGNC ID
7415
RC complex
V
Ensembl gene ID
ENSG00000228253
Ensembl protein ID
ENSP00000355265
Ensembl transcript ID
ENST00000361851
Uniprot ID
P03928
Uniprot name
ATP8_HUMAN
Ncbi gene ID
4509
Ncbi protein ID
YP_003024030.1
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Powered by MitoWheel

Conservation

PhyloP 100v
7.698 Conservation Score
PhyloP 470way
0.742 Conservation Score
PhastCons 100v
1 Conservation Score
PhastCons 470way
0.965 Conservation Score

Pathogenicity predictors

PolyPhen2
Probably damaging Score and details of the predictor
SIFT
Neutral Score and details of the predictor
SIFT4G
Damaging Score and details of the predictor
VEST
Neutral Score and details of the predictor
MitoClass 1
Damaging Score and details of the predictor
SNPDryad
Pathogenic Score and details of the predictor
MutationTaster
.
fathmm
.
AlphaMissense
Likely benign Score and details of the predictor
CADD
Deleterious Score and details of the predictor
PROVEAN
Damaging Score and details of the predictor
Mutation Assessor
Medium Score and details of the predictor
EFIN SP
Neutral Score and details of the predictor
EFIN HD
Damaging Score and details of the predictor
MLC
Deleterious Score and details of the predictor
PANTHER
.
PhD-SNP
.

Pathogenicity meta-predictors

APOGEE1
Pathogenic Score and details of the meta-predictor
APOGEE2
Likely-pathogenic Score and details of the meta-predictor
CAROL
Deleterious Score and details of the meta-predictor
Condel
Neutral Score and details of the meta-predictor
COVEC WMV
Deleterious Score and details of the meta-predictor
MtoolBox
Deleterious Score and details of the meta-predictor
DEOGEN2
.
Meta SNP
.

Cancer-specific predictors

PolyPhen2 transf
Low impact Score and details of the cancer-specific predictor
SIFT transf
Medium impact Score and details of the cancer-specific predictor
MutationAssessor transf
High impact Score and details of the cancer-specific predictor
CHASM
Neutral Score and details of the cancer-specific predictor

Databases of Frequencies and Phenotypes

Clinvar ID
.
Clinvar ALLELEID
.
Clinvar CLNDISDB
.
Clinvar CLNDN
.
Clinvar CLNSIG
.
MITOMAP Allele
8528T>G
MITOMAP Disease Clinical info
.
MITOMAP Disease Status
.
MITOMAP Disease Hom/Het
./.
MITOMAP General GenBank Freq
.
MITOMAP General GenBank Seqs
.
MITOMAP General GenBank Curated refs
.
MITOMAP Variant Class
.
Gnomad AN
0
Gnomad AC hom
0
Gnomad AF hom
0.0
Gnomad AC het
.
Gnomad AF het
.
Gnomad filter
.
HelixMTdb AC hom
0
HelixMTdb AF hom
0.0
HelixMTdb AC het
.
HelixMTdb AF het
0.0
HelixMTdb mean ARF
0.0
HelixMTdb max ARF
.
ToMMo JPN54K AC
.
ToMMo JPN54K AF
.
ToMMo JPN54K AN
.
COSMIC 90
.
dbSNP 156
.

Residue interaction

EVmutation
Site A-B InterP
Site A-B IntraP
ΔΔG intra
ΔΔG intra interface
ΔΔG inter

Compensated Pathogenic Deviations

Frequency
.
AA ref
.
CPD AA alt
.
Aln pos
.
RefSeq protein ID
.
Species name
.
Ncbi taxon ID
.

8528 (T > A)

General info

Mitimpact ID
MI.3
Chr
chrM
Start
8528
Ref
T
Alt
A
Gene symbol
MT-ATP6 Extended gene annotation
Gene position
2
Gene start
8527
Gene end
9207
Gene strand
+
Codon substitution
ATG/AAG
AA pos
1
AA ref
M
AA alt
K
Functional effect
start_lost
OMIM ID
516060
HGVS
NC_012920.1:g.8528T>A
HGNC ID
7414
RC complex
V
Ensembl gene ID
ENSG00000198899
Ensembl protein ID
ENSP00000354632
Ensembl transcript ID
ENST00000361899
Uniprot ID
P00846
Uniprot name
ATP6_HUMAN
Ncbi gene ID
4508
Ncbi protein ID
YP_003024031.1
Powered by NGL Viewer
Powered by MitoWheel

Conservation

PhyloP 100v
7.698 Conservation Score
PhyloP 470way
0.742 Conservation Score
PhastCons 100v
1 Conservation Score
PhastCons 470way
0.965 Conservation Score

Pathogenicity predictors

PolyPhen2
Possibly damaging Score and details of the predictor
SIFT
Deleterious Score and details of the predictor
SIFT4G
Damaging Score and details of the predictor
VEST
Neutral Score and details of the predictor
MitoClass 1
Damaging Score and details of the predictor
SNPDryad
Pathogenic Score and details of the predictor
MutationTaster
Disease Score and details of the predictor
fathmm
Tolerated Score and details of the predictor
AlphaMissense
.
CADD
Deleterious Score and details of the predictor
PROVEAN
Damaging Score and details of the predictor
Mutation Assessor
.
EFIN SP
Neutral Score and details of the predictor
EFIN HD
Damaging Score and details of the predictor
MLC
Deleterious Score and details of the predictor
PANTHER
.
PhD-SNP
.

Pathogenicity meta-predictors

APOGEE1
Pathogenic Score and details of the meta-predictor
APOGEE2
Vus+ Score and details of the meta-predictor
CAROL
Deleterious Score and details of the meta-predictor
Condel
Neutral Score and details of the meta-predictor
COVEC WMV
Deleterious Score and details of the meta-predictor
MtoolBox
Deleterious Score and details of the meta-predictor
DEOGEN2
Tolerated Score and details of the meta-predictor
Meta SNP
.

Cancer-specific predictors

PolyPhen2 transf
.
SIFT transf
.
MutationAssessor transf
.
CHASM
Neutral Score and details of the cancer-specific predictor

Databases of Frequencies and Phenotypes

Clinvar ID
.
Clinvar ALLELEID
.
Clinvar CLNDISDB
.
Clinvar CLNDN
.
Clinvar CLNSIG
.
MITOMAP Allele
8528T>A
MITOMAP Disease Clinical info
.
MITOMAP Disease Status
.
MITOMAP Disease Hom/Het
./.
MITOMAP General GenBank Freq
.
MITOMAP General GenBank Seqs
.
MITOMAP General GenBank Curated refs
.
MITOMAP Variant Class
.
Gnomad AN
0
Gnomad AC hom
0
Gnomad AF hom
0.0
Gnomad AC het
.
Gnomad AF het
.
Gnomad filter
.
HelixMTdb AC hom
0
HelixMTdb AF hom
0.0
HelixMTdb AC het
.
HelixMTdb AF het
0.0
HelixMTdb mean ARF
0.0
HelixMTdb max ARF
.
ToMMo JPN54K AC
.
ToMMo JPN54K AF
.
ToMMo JPN54K AN
.
COSMIC 90
.
dbSNP 156
.

Residue interaction

EVmutation
Site A-B InterP
Site A-B IntraP
ΔΔG intra
ΔΔG intra interface
ΔΔG inter

Compensated Pathogenic Deviations

Frequency
.
AA ref
.
CPD AA alt
.
Aln pos
.
RefSeq protein ID
.
Species name
.
Ncbi taxon ID
.

8528 (T > C)

General info

Mitimpact ID
MI.4
Chr
chrM
Start
8528
Ref
T
Alt
C
Gene symbol
MT-ATP6 Extended gene annotation
Gene position
2
Gene start
8527
Gene end
9207
Gene strand
+
Codon substitution
ATG/ACG
AA pos
1
AA ref
M
AA alt
T
Functional effect
start_lost
OMIM ID
516060
HGVS
NC_012920.1:g.8528T>C
HGNC ID
7414
RC complex
V
Ensembl gene ID
ENSG00000198899
Ensembl protein ID
ENSP00000354632
Ensembl transcript ID
ENST00000361899
Uniprot ID
P00846
Uniprot name
ATP6_HUMAN
Ncbi gene ID
4508
Ncbi protein ID
YP_003024031.1
Powered by NGL Viewer
Powered by MitoWheel

Conservation

PhyloP 100v
7.698 Conservation Score
PhyloP 470way
0.742 Conservation Score
PhastCons 100v
1 Conservation Score
PhastCons 470way
0.965 Conservation Score

Pathogenicity predictors

PolyPhen2
Possibly damaging Score and details of the predictor
SIFT
Deleterious Score and details of the predictor
SIFT4G
Damaging Score and details of the predictor
VEST
Neutral Score and details of the predictor
MitoClass 1
Damaging Score and details of the predictor
SNPDryad
Pathogenic Score and details of the predictor
MutationTaster
Disease automatic Score and details of the predictor
fathmm
Tolerated Score and details of the predictor
AlphaMissense
.
CADD
Deleterious Score and details of the predictor
PROVEAN
Damaging Score and details of the predictor
Mutation Assessor
.
EFIN SP
Neutral Score and details of the predictor
EFIN HD
Damaging Score and details of the predictor
MLC
Deleterious Score and details of the predictor
PANTHER
.
PhD-SNP
.

Pathogenicity meta-predictors

APOGEE1
Pathogenic Score and details of the meta-predictor
APOGEE2
Likely-pathogenic Score and details of the meta-predictor
CAROL
Deleterious Score and details of the meta-predictor
Condel
Neutral Score and details of the meta-predictor
COVEC WMV
Deleterious Score and details of the meta-predictor
MtoolBox
Deleterious Score and details of the meta-predictor
DEOGEN2
Tolerated Score and details of the meta-predictor
Meta SNP
.

Cancer-specific predictors

PolyPhen2 transf
.
SIFT transf
.
MutationAssessor transf
.
CHASM
Neutral Score and details of the cancer-specific predictor

Databases of Frequencies and Phenotypes

Clinvar ID
9640
Clinvar ALLELEID
24679
Clinvar CLNDISDB
Mondo:mondo:0044970, medgen:c0751651, orphanet:68380;

human phenotype ontology:hp:0005152, mondo:mondo:0010771, medgen:c1708371, omim:500000, orphanet:137675;

mondo:mondo:0010777, medgen:c2748884, omim:500006
Clinvar CLNDN
Mitochondrial disease;

histiocytoid cardiomyopathy;

cardiomyopathy, infantile hypertrophic
Clinvar CLNSIG
Likely pathogenic
MITOMAP Allele
8528T>C
MITOMAP Disease Clinical info
Infantile cardiomyopathy / hyperammonemia
MITOMAP Disease Status
Cfrm [lp]
MITOMAP Disease Hom/Het
+/+
MITOMAP General GenBank Freq
0.0%
MITOMAP General GenBank Seqs
0
MITOMAP General GenBank Curated refs
26803244 30642647 19188198 27409572 26741492 34298071 33180048 30763462 21457906
MITOMAP Variant Class
disease
Gnomad AN
0
Gnomad AC hom
0
Gnomad AF hom
0.0
Gnomad AC het
.
Gnomad AF het
.
Gnomad filter
.
HelixMTdb AC hom
0
HelixMTdb AF hom
0.0
HelixMTdb AC het
.
HelixMTdb AF het
0.0
HelixMTdb mean ARF
0.0
HelixMTdb max ARF
.
ToMMo JPN54K AC
.
ToMMo JPN54K AF
.
ToMMo JPN54K AN
.
COSMIC 90
.
dbSNP 156
rs387906422

Residue interaction

EVmutation
Site A-B InterP
Site A-B IntraP
ΔΔG intra
ΔΔG intra interface
ΔΔG inter

Compensated Pathogenic Deviations

Frequency
.
AA ref
.
CPD AA alt
.
Aln pos
.
RefSeq protein ID
.
Species name
.
Ncbi taxon ID
.
~ 8528 (T/C) 8528 (T/G) 8528 (T/A) 8528 (T/C)
~ 8528 (TGA/CGA) 8528 (TGA/GGA) 8528 (ATG/AAG) 8528 (ATG/ACG)
MitImpact id MI.1789 MI.1788 MI.3 MI.4
Chr chrM chrM chrM chrM
Start 8528 8528 8528 8528
Ref T T T T
Alt C G A C
Gene symbol MT-ATP8 MT-ATP8 MT-ATP6 MT-ATP6
Extended annotation mitochondrially encoded ATP synthase membrane subunit 8 mitochondrially encoded ATP synthase membrane subunit 8 mitochondrially encoded ATP synthase membrane subunit 6 mitochondrially encoded ATP synthase membrane subunit 6
Gene position 163 163 2 2
Gene start 8366 8366 8527 8527
Gene end 8572 8572 9207 9207
Gene strand + + + +
Codon substitution TGA/CGA TGA/GGA ATG/AAG ATG/ACG
AA position 55 55 1 1
AA ref W W M M
AA alt R G K T
Functional effect general missense missense start_lost start_lost
Functional effect detailed missense missense start_lost start_lost
OMIM id 516070 516070 516060 516060
HGVS NC_012920.1:g.8528T>C NC_012920.1:g.8528T>G NC_012920.1:g.8528T>A NC_012920.1:g.8528T>C
HGNC id 7415 7415 7414 7414
Respiratory Chain complex V V V V
Ensembl gene id ENSG00000228253 ENSG00000228253 ENSG00000198899 ENSG00000198899
Ensembl transcript id ENST00000361851 ENST00000361851 ENST00000361899 ENST00000361899
Ensembl protein id ENSP00000355265 ENSP00000355265 ENSP00000354632 ENSP00000354632
Uniprot id P03928 P03928 P00846 P00846
Uniprot name ATP8_HUMAN ATP8_HUMAN ATP6_HUMAN ATP6_HUMAN
Ncbi gene id 4509 4509 4508 4508
Ncbi protein id YP_003024030.1 YP_003024030.1 YP_003024031.1 YP_003024031.1
PhyloP 100V 7.698 7.698 7.698 7.698
PhyloP 470Way 0.742 0.742 0.742 0.742
PhastCons 100V 1 1 1 1
PhastCons 470Way 0.965 0.965 0.965 0.965
PolyPhen2 probably_damaging probably_damaging possibly_damaging possibly_damaging
PolyPhen2 score 1.0 0.98 0.8 0.8
SIFT neutral neutral deleterious deleterious
SIFT score 0.31 0.34 0 0
SIFT4G Damaging Damaging Damaging Damaging
SIFT4G score 0.0 0.0 0.0 0.0
VEST Neutral Neutral Neutral Neutral
VEST pvalue 0.15055088 0.13200123 0.25 0.47
VEST FDR 0.85 0.85 0.65 0.65
Mitoclass.1 damaging damaging damaging damaging
SNPDryad Pathogenic Pathogenic Pathogenic Pathogenic
SNPDryad score 0.97 0.93 0.99 0.97
MutationTaster . . Disease Disease automatic
MutationTaster score . . 1 1
MutationTaster converted rankscore . . 0.81001 0.81001
MutationTaster model . . complex_aae complex_aae
MutationTaster AAE . . N2T N2T
fathmm . . Tolerated Tolerated
fathmm score . . 4.64 4.63
fathmm converted rankscore . . 0.01799 0.01817
AlphaMissense likely_pathogenic likely_benign . .
AlphaMissense score 0.7923 0.3215 . .
CADD Deleterious Deleterious Deleterious Deleterious
CADD score 3.65294 3.958969 6.259636 3.65294
CADD phred 23.2 23.6 28.9 23.2
PROVEAN Damaging Damaging Damaging Damaging
PROVEAN score -12.74 -12.02 -4.89 -4.97
MutationAssessor . medium . .
MutationAssessor score . 3.38 . .
EFIN SP Neutral Neutral Neutral Neutral
EFIN SP score 0.85 0.84 0.614 0.704
EFIN HD Damaging Damaging Damaging Damaging
EFIN HD score 0.06 0.104 0.09 0.126
MLC Deleterious Deleterious Deleterious Deleterious
MLC score 0.7 0.7 0.7 0.7
PANTHER score . . . .
PhD-SNP score . . . .
APOGEE1 Pathogenic Pathogenic Pathogenic Pathogenic
APOGEE1 score 0.58 0.64 0.58 0.63
APOGEE2 Likely-pathogenic Likely-pathogenic VUS+ Likely-pathogenic
APOGEE2 score 0.841959764587885 0.820374350074967 0.565745889740842 0.759827033070099
CAROL deleterious deleterious deleterious deleterious
CAROL score 1 0.98 1 1
Condel neutral neutral neutral neutral
Condel score 0.16 0.18 0.1 0.1
COVEC WMV deleterious deleterious deleterious deleterious
COVEC WMV score 2 2 3 3
MtoolBox deleterious deleterious deleterious deleterious
MtoolBox DS 0.9 0.87 0.73 0.76
DEOGEN2 . . Tolerated Tolerated
DEOGEN2 score . . 0.238148 0.311115
DEOGEN2 converted rankscore . . 0.60599 0.68302
Meta-SNP . . . .
Meta-SNP score . . . .
PolyPhen2 transf low impact low impact . .
PolyPhen2 transf score -3.6 -2.36 . .
SIFT_transf medium impact medium impact . .
SIFT transf score 0.1 0.13 . .
MutationAssessor transf high impact high impact . .
MutationAssessor transf score 2.07 2.07 . .
CHASM Neutral Neutral Neutral Neutral
CHASM pvalue 0.08 0.06 0.42 0.24
CHASM FDR 0.85 0.85 0.9 0.9
ClinVar id 9640.0 . . 9640.0
ClinVar Allele id 24679.0 . . 24679.0
ClinVar CLNDISDB MONDO:MONDO:0044970,MedGen:C0751651,Orphanet:68380|Human_Phenotype_Ontology:HP:0005152,MONDO:MONDO:0010771,MedGen:C1708371,OMIM:500000,Orphanet:137675|MONDO:MONDO:0010777,MedGen:C2748884,OMIM:500006 . . MONDO:MONDO:0044970,MedGen:C0751651,Orphanet:68380|Human_Phenotype_Ontology:HP:0005152,MONDO:MONDO:0010771,MedGen:C1708371,OMIM:500000,Orphanet:137675|MONDO:MONDO:0010777,MedGen:C2748884,OMIM:500006
ClinVar CLNDN Mitochondrial_disease|Histiocytoid_cardiomyopathy|Cardiomyopathy,_infantile_hypertrophic . . Mitochondrial_disease|Histiocytoid_cardiomyopathy|Cardiomyopathy,_infantile_hypertrophic
ClinVar CLNSIG Likely_pathogenic . . Likely_pathogenic
MITOMAP Disease Clinical info Infantile cardiomyopathy / hyperammonemia . . Infantile cardiomyopathy / hyperammonemia
MITOMAP Disease Status Cfrm [LP] . . Cfrm [LP]
MITOMAP Disease Hom/Het +/+ ./. ./. +/+
MITOMAP General GenBank Freq 0.0% . . 0.0%
MITOMAP General GenBank Seqs 0 . . 0
MITOMAP General Curated refs 26803244;30642647;19188198;27409572;26741492;34298071;33180048;30763462;21457906 . . 26803244;30642647;19188198;27409572;26741492;34298071;33180048;30763462;21457906
MITOMAP Variant Class disease . . disease
gnomAD 3.1 AN . . . .
gnomAD 3.1 AC Homo . . . .
gnomAD 3.1 AF Hom . . . .
gnomAD 3.1 AC Het . . . .
gnomAD 3.1 AF Het . . . .
gnomAD 3.1 filter . . . .
HelixMTdb AC Hom . . . .
HelixMTdb AF Hom . . . .
HelixMTdb AC Het . . . .
HelixMTdb AF Het . . . .
HelixMTdb mean ARF . . . .
HelixMTdb max ARF . . . .
ToMMo 54KJPN AC . . . .
ToMMo 54KJPN AF . . . .
ToMMo 54KJPN AN . . . .
COSMIC 90 . . . .
dbSNP 156 id . . . rs387906422
For more info, please check the output legend.
ΔΔG values >±0.61 Kcal/mol are indicative of disrupting variants.
ΔΔG values close to zero (<±0.1 Kcal/mol) are indicative of possibly
compensating double mutants.
For more info, please check the output legend.
ΔΔG values >±0.61 Kcal/mol are indicative of disrupting variants.
ΔΔG values close to zero (<±0.1 Kcal/mol) are indicative of possibly
compensating double mutants.
For more info, please check the output legend.
ΔΔG values >±0.61 Kcal/mol are indicative of disrupting variants.
ΔΔG values close to zero (<±0.1 Kcal/mol) are indicative of possibly
compensating double mutants.
For more info, please check the output legend.
For more info, please check the output legend.
0
Details:
0
Score:  
0
  [min -20, max 10]
  • Predicted accelerated evolution:  score <= 0
  • Conserved:  score > 0
Score:  
0
  [min -20, max 12]
  • Predicted accelerated evolution:  score <= 0
  • Conserved:  score > 0
Score:  
0
  [min 0, max 1]
  • Non-conserved:  score <= 0.7
  • Conserved:  score > 0.7 (soft threshold)
Score:  
0
  [min 0, max 1]
  • Non-conserved:  score <= 0.7
  • Conserved:  score > 0.7 (soft threshold)
Score:  
0
  [min 0, max 1]
  • Neutral:  score <= 0.15
  • Possibly damaging:  0.15 < score <= 0.85
  • Probably damaging:  score > 0.85
Score:  
0
  [min 0, max 1]
  • Neutral:  score > 0.05
  • Deleterious:  score <= 0.05
Score:  
0
  [min 0, max 1]
  • Neutral:  score > 0.05
  • Deleterious:  score <= 0.05
Score:  
0
  [min -16.13, max 10.64]
  • Neutral:  score > 1.5
  • Deleterious:  score <= 1.5
Score:  
0
  [min 0.0, max 1.0]
  • Likely benign:  score <= 0.34
  • Ambiguous:  0.34 < score < 0.56
  • Likely pathogenic:  score >= 0.56
Score:  
0
  [min -14, max 14]
  • Neutral:  score > -2.5
  • Deleterious:  score <= -2.5 (soft threshold)
Score:  
0
  [min -6, max 6]
  • Neutral:  score <= 0.8
  • Low impact:  0.8 < score <= 1.9
  • Medium impact:  1.9 < score <= 3.5
  • High impact:  score > 3.5
Score:  
0
  [min 0, max 1]
  • Neutral:  score > 0.6
  • Damaging:  score <= 0.6
Score:  
0
  [min 0, max 1]
  • Neutral:  score > 0.28
  • Damaging:  score <= 0.28
Phred score:  
0
  [min 0, max Unlimited]
  • Neutral:  score < 20 (soft threshold)
  • Deleterious:  score >= 20
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5 (soft threshold)
  • Deleterious:  score >= 0.5
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5
  • Disease:  score >= 0.5
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5
  • Disease:  score >= 0.5
Score:  
0
  [min 0, max 1]
  • Polymorphism:  score < 0.5
  • Disease causing:  score >= 0.5
P-value:  
0
  [min 0, max 1]
  • Neutral:  p-value > 0.05
  • Pathogenic:  p-value <= 0.05
Score:  
0
  [min 0, max 1]
No hard-thresholds were indicated by authors (ref). Indicatively:
  • Neutral:  score < 0.9
  • Pathogenic:  score >= 0.9
No score. Categorical only
Please refer to Additional File 14: Table S10 for further details.
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.98
  • Deleterious:  score >= 0.98
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5
  • Disease:  score >= 0.5
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5
  • Deleterious:  score >= 0.5
Score:  
0
  [min -6, max 6]
  • Neutral:  score < 0
  • Deleterious:  score > 0
  • Inaccurate prediction:  score = 0
Score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.5
  • Deleterious:  score >= 0.5
DS score:  
0
  [min 0, max 1]
  • Neutral:  score < 0.43
  • Deleterious:  score >= 0.43
Pathogenicity score:  
0
  [min 0, max 1]
  • Neutral:  score ≤ 0.5
  • Pathogenic:  score > 0.5


Pathogenicity score for this variant:  
0
  [min 0, max 1]
ACMG-AMP curations for mitochondrial variants should use the raw scores. Standalone probabilities are shown below:
  • Benign:  score ≤ 0.062 (prob. ≤ 0.001)
  • Likely-benign:  0.062 < score ≤ 0.265 (0.001 < prob. ≤ 0.1)
  • Low-scoring VUS (VUS-):  0.265 < score ≤ 0.396 (0.1 < prob. ≤ 0.33)
  • VUS:  0.396 < score ≤ 0.544 (0.33 < prob. ≤ 0.66)
  • High-scoring VUS (VUS+):  0.544 < score < 0.716 (0.66 < prob. < 0.9)
  • Likely-pathogenic:  0.716 ≤ score < 0.907 (0.9 ≤ prob. < 0.99)
  • Pathogenic:  score ≥ 0.907 (prob. ≥ 0.99)
Score:  
0
  [min -5, max 5]
  • Low impact:  score <= -1 (soft threshold)
  • Medium impact:  -1 < score < 1.5 (soft threshold)
  • High impact:  score >= 1.5 (soft threshold)
Score:  
0
  [min -5, max 5]
  • Low impact:  score <= -1
  • Medium impact:  -1 < score < 2 (soft threshold)
  • High impact:  score >= 2 (soft threshold)
Score:  
0
  [min -5, max 5]
  • Low impact:  score <= -1
  • Medium impact:  -1 < score < 2 (soft threshold)
  • High impact:  score >= 2 (soft threshold)
P-value:  
0
  [min 0, max 1]
  • Neutral:  FDR > 0.2
  • Driver:  FDR <= 0.2
The frequency of a CPD variant is proportional to the
number of aligned orthologous sequences that
carry a specific human pathogenic variant as
wild-type amino acid on the total number of aligned
sequences.

For more info, please check the output legend