Variant ID | 31421 |
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Entrez Gene ID | 6299 |
Gene | SALL1 (GeneCards) |
Location | hg19 16:51174702-51174702
hg38 16:51140791-51140791 |
Disease | Asymptomatic |
Method | NGS gene panel |
Mutation(HGVS format) | NC_000016.9:g.51174702 G>A (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 477 |
Amino acid changes in protein | F > F |
Position in cDNA | 1431 |
Changes in cDNA | C > T |
mRNA accession | NA |
mRNA length | NA |
Reference length | 90354753 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 1.788 |
CADD Raw score (version 1.3) | 0.326482 (Deleterious) |
FATHMM raw prediction score | 0.95226 (Tolerated) |
Deleterious probability by DeFine | 0.9669 (Deleterious) |
Entrez Gene ID | 6299 (NCBI Gene) |
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Official Gene Symbol | SALL1 (GeneCards) |
Number of variants in SALL1 in this database | 95 (view all the variants) |
Full name | spalt like transcription factor 1 |
Band | 16q12.1 |
Other IDs | Vega: OTTHUMG00000133176 OMIM: 602218 HGNC: HGNC:10524 Ensembl: ENSG00000103449 |
Other names | TBS, HSAL1, Sal-1, ZNF794, HEL-S-89 |
Summary | The protein encoded by this gene is a zinc finger transcriptional repressor and may be part of the NuRD histone deacetylase complex (HDAC). Defects in this gene are a cause of Townes-Brocks syndrome (TBS) as well as bronchio-oto-renal syndrome (BOR). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Individual ID | 25999502.02 (view all the variants in this individual) |
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Pubmed ID | 25999502 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 25999502 |
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Title | High burden and pervasive positive selection of somatic mutations in normal human skin |
Journal | Science |
Publication date | 2015.05 |
Disease | Asymptomatic |
Number of cases | Male cases: 1; Female cases: 3; |