Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


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

Most severe consequence
Evidence status

Clinical significance

This variation has 3 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 3 phenotypes and is mentioned in 1 citation.

Variation displays