Overview

Variant ID 34304
Entrez Gene ID 2272
Gene FHIT (GeneCards)
Location hg19 3:60661591-60661591
hg38 3:60675858-60675858
Disease Asymptomatic
Method Whole Genome Sequencing Ion Torrent PGM Sequencing
Mutation(HGVS format) NC_000003.11:g.60661591 T>A (Genome Assembly: hg19)

Other information

Exon or Intron intron
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 198022430

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.002
CADD Raw score (version 1.3) 0.363965 (Deleterious)
FATHMM raw prediction score 0.13733 (Tolerated)
Deleterious probability by DeFine 0.4929 (Neutral)
Entrez Gene ID 2272 (NCBI Gene)
Official Gene Symbol FHIT (GeneCards)
Number of variants in FHIT in this database 27 (view all the variants)
Full name fragile histidine triad
Band 3p14.2
Other IDs Vega: OTTHUMG00000158591
OMIM: 601153
HGNC: HGNC:3701
Ensembl: ENSG00000189283
Other names FRA3B, AP3Aase
Summary The protein encoded by this gene is a P1-P3-bis(5'-adenosyl) triphosphate hydrolase involved in purine metabolism. This gene encompasses the common fragile site FRA3B on chromosome 3, where carcinogen-induced damage can lead to translocations and aberrant transcripts. In fact, aberrant transcripts from this gene have been found in about half of all esophageal, stomach, and colon carcinomas. The encoded protein is also a tumor suppressor, as loss of its activity results in replication stress and DNA damage. [provided by RefSeq, Aug 2017]

Individual #1

Individual ID 24760347.01 (view all the variants in this individual)
Pubmed ID 24760347
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 24760347

Pubmed ID 24760347
Title Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
Journal Genome Research
Publication date 2014.04
Disease Asymptomatic
Number of cases Female cases: 1;