Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 11:2160956 (forward strand) | View in location tab


with COSMIC COSM3931294 (G/A), COSM3931293 (G/A) ; HGMD-PUBLIC CM082897

Most severe consequence
Missense variant
Evidence status

Clinical significance


Uniprot VAR_063721

This variant has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays