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: T | Ambiguity code: N | MAF: 0.36 (G)

Chromosome 12:12718165 (forward strand) | View in location tab


with COSMIC COSM4146812 (T/G) ; HGMD-PUBLIC CM033961

Most severe consequence
Missense variant
Evidence status


This variant has 5 synonyms - Show

HGVS names

This variant has 21 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 15 transcripts, 1 regulatory feature, has 4141 sample genotypes and is mentioned in 24 citations.

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