Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 4:41260751 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3603776 ; HGMD-PUBLIC CM981986

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5978

HGVS names

This variant has 32 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and is associated with 2 phenotypes.

Variant displays