Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.21 (C)

Chromosome 17:61456507 (forward strand) | View in location tab


with COSMIC COSM3755734 (G/C)

Most severe consequence
Evidence status


Uniprot VAR_020251

This variation has 6 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 1367 individual genotypes and is mentioned in 5 citations.

Variation displays