Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 3:122284413 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3586280 ; HGMD-PUBLIC CM021251 ; PhenCode CASRdb_c.2459C>G (C/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 10003, 2010_April_001_051_CASR_601199_0038

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays