Overview

Variant ID 873
Entrez Gene ID 196385
Gene DNAH10 (GeneCards)
Location hg19 12:124411356-124411356
hg38 12:123926809-123926809
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000012.11:g.124411356 G>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 3914
Amino acid changes in protein G > S
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 133851895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.8791
CADD Raw score (version 1.3) 6.475506 (Deleterious)
FATHMM raw prediction score 0.98266 (Tolerated)
SIFT score 0.024 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 3.46 (Deleterious)
PROVEAN score -6 (Deleterious)
MetaSVM score -0.588 (Tolerated)
MetaLR score 0.158 (Tolerated)
MCAP score 0.045 (Deleterious)
FitCons score 0.549 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 3.86
PhyloP score based on multiple alignment of 100 vertebrates 10.003
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 14.006
Deleterious probability by iFish2 0.5572 (Deleterious)
Deleterious probability by DeFine 0.964 (Deleterious)
Entrez Gene ID 196385 (NCBI Gene)
Official Gene Symbol DNAH10 (GeneCards)
Number of variants in DNAH10 in this database 3 (view all the variants)
Full name dynein axonemal heavy chain 10
Band 12q24.31
Other IDs Vega: OTTHUMG00000154477
OMIM: 605884
HGNC: HGNC:2941
Ensembl: ENSG00000197653
Other names None
Summary Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH10 is an inner arm dynein heavy chain (Maiti et al., 2000 [PubMed 11175280]).[supplied by OMIM, Mar 2008]

Individual #1

Individual ID 27788131.01 (view all the variants in this individual)
Pubmed ID 27788131
Whose mosaic mutation Normal  
Phenotype 1  
Disease Human Skin Fibroblasts (view all the variants in this disease)
OMIM ID 120353

Publication #1: 27788131

Pubmed ID 27788131
Title The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts.
Journal PLoS Genetics
Publication date 2016.10
Disease Human Skin Fibroblasts
Population Caucasian
Number of cases Male cases: 2;