Original source

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

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

Chromosome 13:113122874 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM025192

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014162

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays