Original source

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

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

Chromosome 12:21635657 (forward strand) | View in location tab

Co-located

with COSMIC COSM3931606 (T/C)

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2504 individual genotypes.

Variation displays