Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (A)

Chromosome 17:7078078 (forward strand) | View in location tab


with COSMIC COSM4130542 (A/G), COSM4130543 (A/G)

Most severe consequence
Missense variant
Evidence status


This variant has 7 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3797 sample genotypes.

Variant displays