Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (T)

Chromosome 11:34970180 (forward strand) | View in location tab


with COSMIC COSM4145674 (T/C), COSM4145675 (T/C)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3794 sample genotypes.

Variant displays