Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)

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


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

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs58894804

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

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

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 3692 sample genotypes and is mentioned in 4 citations.

Variant displays