Original source

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

This variant has 4 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2583 sample genotypes.

Variant displays