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: 0.13 (C)

Chromosome 15:74720644 (forward strand) | View in location tab


with COSMIC COSM3999600 (T/C) ; HGMD-PUBLIC CM940327

Most severe consequence
Missense variant
Evidence status


This variant has 5 synonyms - Show

HGVS names

This variant has 39 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 30 transcripts, has 3688 sample genotypes and is mentioned in 105 citations.

Variant displays