Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.42 (A)

Chromosome 7:99903288 (forward strand) | View in location tab


with COSMIC COSM3762926 (A/G), COSM3762927 (A/G)

Most severe consequence
Synonymous variant
Evidence status


This variant has 5 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 4339 sample genotypes.

Variant displays