Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 16:86567632 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM002969

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 11036, 2010_April_001_032_FOXC2_602402_0001

HGVS names

This variant has 4 HGVS names - Hide

16:g.86567632C>G
ENST00000320354.5:c.297C>G
ENSP00000326371.4:p.Tyr99Ter
ENST00000563280.1:n.130G>C

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays