Original source

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

T/C/G | Ancestral: C | Ambiguity code: B | MAF: 0.20 (T)

Chromosome 15:38351373 (forward strand) | View in location tab


with COSMIC COSM3999508 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3800 sample genotypes and is associated with 2 phenotypes.

Variant displays