Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 11:116837100 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4662471 ; HGMD-PUBLIC CM900015

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays