Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.20 (G)

Chromosome 15:38322324 (forward strand) | View in location tab


with COSMIC COSM4148687 (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NM_152594.2:c.291G>A

This variant has 4 HGVS names - click the plus to show

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

About this variant

This variant overlaps 3 transcripts, has 3772 sample genotypes and is associated with 2 phenotypes.

Variant displays