Original source

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

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

Chromosome 1:77929455 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_059414

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 726 sample genotypes.

Variant displays