Original source

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

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

Chromosome 6:3105788 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_058285

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 262 sample genotypes.

Variant displays