Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 15:34793398 (forward strand) | View in location tab


with COSMIC COSM960888 (C/T) ; HGMD-PUBLIC CM003400 ; PhenCode FHC0690 (C/T)

Most severe consequence
Evidence status

Clinical significance


LSDB ACTC_301G_A_081610, 33370

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, is associated with 4 phenotypes and is mentioned in 5 citations.

Variation displays