Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.17 (C)

Chromosome 14:64233327 (forward strand) | View in location tab


with COSMIC COSM3999325 (T/C) ; HGMD-PUBLIC CS067819

Most severe consequence
Evidence status


Archive dbSNP rs58894804

This variation has 13 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 2284 individual genotypes and is mentioned in 3 citations.

Variation displays