Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A/T | Ancestral: C | Ambiguity code: H

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


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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays