Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.06 (G)

Chromosome 16:47663707 (forward strand) | View in location tab


with COSMIC COSM1629903 (A/T), COSM1629904 (A/T), COSM1629902 (A/T) ; HGMD-PUBLIC CM031328

Most severe consequence
Missense variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3157 sample genotypes.

Variant displays