Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (C)
Location

Chromosome 15:74044292 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754465 (T/C)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3651 individual genotypes, is associated with 3 phenotypes and is mentioned in 2 citations.

Variation displays