Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 21:45990414 (forward strand) | View in location tab

Co-located

with COSMIC COSM4135068 (G/A)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_058220

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays