Overview

Variant ID 13790
Entrez Gene ID 203328
Gene SUSD3 (GeneCards)
Location hg19 9:95835732-95835732
hg38 9:93073450-93073450
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000009.11:g.95835732 G>C (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 141213431

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.6098
CADD Raw score (version 1.3) -0.755378 (Deleterious)
FATHMM raw prediction score 0.06889 (Tolerated)
Deleterious probability by DeFine 0.1564 (Neutral)
Entrez Gene ID 203328 (NCBI Gene)
Official Gene Symbol SUSD3 (GeneCards)
Number of variants in SUSD3 in this database 1 (view all the variants)
Full name sushi domain containing 3
Band 9q22.31
Other IDs Vega: OTTHUMG00000020241
OMIM: 616429
HGNC: HGNC:28391
Ensembl: ENSG00000157303
Other names None
Summary None

Individual #1

Individual ID 29217584.23 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;