Original source

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

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

Chromosome 1:102878027 (forward strand) | View in location tab

Most severe consequence
Missense variant

Uniprot VAR_047728

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 263 sample genotypes.

Variant displays