Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 12:110915715 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_029449

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 5 transcripts, has 271 sample genotypes and is mentioned in 1 citation.

Variant displays