Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.17 (T)

Chromosome 11:45953579 (forward strand) | View in location tab


with COSMIC COSM3752369 (C/T), COSM3752368 (C/T)

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 5 transcripts and has 3716 sample genotypes.

Variant displays