Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (G)

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


with COSMIC COSM4148687 (G/A)

Most severe consequence
Evidence status

Clinical significance


LSDB NM_152594.2:c.291G>A

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

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

About this variant

This variant overlaps 3 transcripts, has 2374 individual genotypes and is associated with 2 phenotypes.

Variation displays