Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 2:162268127 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM091739

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

2:g.162268127T>C
ENST00000263642.2:c.2767A>G
ENSP00000263642.2:p.Ile923Val

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2527 individual genotypes and is mentioned in 14 citations.

Variation displays