Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 12:40363526 (forward strand) | View in location tab

Co-located

with COSMIC COSM431073 (G/A), COSM431072 (G/A) ; HGMD-PUBLIC CM057191

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2506 individual genotypes, is associated with 4 phenotypes and is mentioned in 11 citations.

Variation displays