Original source

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

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

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

Co-located

with COSMIC COSM1635939 (G/A) ; HGMD-PUBLIC CM063198, CM050757

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5763, 5765

This variant has 20 HGVS names - click the plus to show

About this variant

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

Variant displays