Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 8:31032356 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_053614

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays