Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.13 (A)
Location

Chromosome 4:47320202 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760642 (C/A)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 5688 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays