Original source

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

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

Chromosome 11:2160835 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082896

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_063729

This variant has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays