Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.30 (C)

Chromosome 15:63059641 (forward strand) | View in location tab


with COSMIC COSM3754386 (C/A), COSM3754388 (C/A), COSM3754390 (C/A), COSM3754387 (C/A), COSM3754389 (C/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 32 transcripts, has 2414 individual genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variation displays