This variant has been flagged

Variation has more than 3 different alleles

Original source

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

T/A/C/G | Ancestral: G | Ambiguity code: N | MAF: 0.32 (T)

Chromosome 8:132888007 (forward strand) | View in location tab


with COSMIC COSM4162675 (T/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 7 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4301 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays