Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 16:86567709 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021602

Most severe consequence
Clinical significance

Synonyms

LSDB 11047

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

16:g.86567709C>T
ENST00000320354.5:c.374C>T
ENSP00000326371.4:p.Ser125Leu
ENST00000563280.1:n.53G>A

Variation displays