Original source

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

T/A/C | Ancestral: T | Ambiguity code: H

Chromosome 11:119278181 (forward strand) | View in location tab


with COSMIC COSM34053 (T/G), COSM34052 (T/C) ; HGMD-PUBLIC CM099544, CM105459

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variant displays