Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)

Chromosome 20:23637790 (forward strand) | View in location tab


with COSMIC COSM3749695 (C/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2505 sample genotypes, is associated with 2 phenotypes and is mentioned in 8 citations.

Variant displays