Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 15:63044030 (forward strand) | View in location tab

Co-located

with COSMIC COSM1230146 (G/A), COSM1230147 (G/A) ; HGMD-PUBLIC CM014115

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 50 HGVS names - click the plus to show

About this variant

This variant overlaps 53 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays