Original source

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

Alleles
C/G|Ambiguity code: S|MAF: 0.03 (G)
Location

Chromosome 22:23314599 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3785508

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_041896

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays