Original source

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

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

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

Most severe consequence
Missense variant
Evidence status


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