Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 20:44118607 (forward strand) | View in location tab

Co-located

with COSMIC COSM1411944 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3725 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays