Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A/C|Ancestral: G|Ambiguity code: V

Chromosome 9:99149253 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1635939 ; HGMD-PUBLIC CM050757, CM063198

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 5763, 5765

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 4 phenotypes.

Variant displays