Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

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

Co-located

with HGMD-PUBLIC CM109189

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014609

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, 2 regulatory features and is mentioned in 2 citations.

Variant displays