Original source

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

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

Chromosome 11:116836061 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM109189

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014609

HGVS names

This variant has 28 HGVS names - Show

About this variant

This variant overlaps 22 transcripts, 2 regulatory features and is mentioned in 2 citations.

Variant displays