Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)

Chromosome 17:61480239 (forward strand) | View in location tab


with COSMIC COSM3755736 (C/T)

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3726 sample genotypes and is mentioned in 4 citations.

Variant displays