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 4:186210508 (forward strand)|View in location tab

Co-located variants

COSMIC COSM586929 ; HGMD-PUBLIC CM053829

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NM_207352.3:c.1445C>A

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 1 phenotype.

Variant displays