Variant ID | 13790 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217584.23 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
OMIM ID | 278700 |
Pubmed ID | 29217584 |
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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; |