Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_ImmunoChip, Illumina_HumanOmni5

Variation displays