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

Chromosome 3:8745579 (forward strand) | View in location tab


with COSMIC COSM377617 (C/A) ; PhenCode CAV3:c.168C>A (C/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays