Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

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

Co-located

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

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

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

About this variant

This variant overlaps 7 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays