Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 1:16997049 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_058454

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and is mentioned in 1 citation.

Variant displays