Original source

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

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

Chromosome 18:51065521 (forward strand) | View in location tab


with COSMIC COSM1150607 (G/A) ; HGMD-PUBLIC CM024126

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, is associated with 6 phenotypes and is mentioned in 2 citations.

Variant displays