Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Co-located

with HGMD-PUBLIC CM002969

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11036, 2010_April_001_032_FOXC2_602402_0001

This variation has 4 HGVS names - click the plus to show

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

Variation displays