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 14:20472366 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981389 ; PhenCode NPbase_D0064:g.3957C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4324, 2010_April_001_039_NP_164050_0008

This variation has 14 HGVS names - click the plus to show

14:g.20472366C>T
ENST00000554065.1:c.-168C>T
ENST00000553418.3:c.70C>T
ENSP00000450663.1:p.Arg24Ter
ENST00000557229.3:n.189C>T
ENST00000553591.1:c.187C>T
ENSP00000452421.1:p.Arg63Ter
ENST00000556293.3:n.189C>T
ENST00000554056.3:n.181C>T
ENST00000361505.7:c.70C>T
ENSP00000354532.5:p.Arg24Ter
LRG_91:g.7984C>T
LRG_91t1.1:c.70C>T
LRG_91p1.1:p.Lys22Asn

Variation displays