Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 13:51946445 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM960128

Most severe consequence
 
Stop lost
Evidence status

Synonyms

Uniprot VAR_010013

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and is associated with 1 phenotype.

Variant displays