Original source

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

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

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

Co-located variants

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

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

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 2 phenotypes and is mentioned in 1 citation.

Variant displays