Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (C)
Location

Chromosome 4:146639259 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760418 (T/C)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_059321

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

This variant has assays on 6 chips - click the plus to show

About this variant

Variant displays