Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 4:73740676 (forward strand) | View in location tab

Co-located

with COSMIC COSM3781187 (C/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4986969

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2506 individual genotypes and is mentioned in 1 citation.

Variation displays