Original source

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

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

Chromosome 9:121310819 (forward strand) | View in location tab


with COSMIC COSM1459756 (G/A), COSM1459755 (G/A) ; HGMD-PUBLIC CM910196, CM920315

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 56 HGVS names - click the plus to show

About this variant

This variant overlaps 34 transcripts and is associated with 3 phenotypes.

Variation displays