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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

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