Original source

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

C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.27 (T)

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


with COSMIC COSM1411944 (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3725 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays