Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)

Chromosome 2:219418537 (forward strand) | View in location tab


with COSMIC COSM3757962 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2509 sample genotypes and is associated with 2 phenotypes.

Variant displays