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 15:25340219 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981985

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_049_UBE3A_601623_0005, 10351

This variation has 17 HGVS names - click the plus to show

15:g.25340219C>T
ENST00000614096.1:c.2364G>A
ENSP00000481796.1:p.Trp788Ter
ENST00000554726.1:n.246-51377C>T
ENST00000566215.2:c.2304G>A
ENSP00000457771.1:p.Trp768Ter
ENST00000397954.3:c.2373G>A
ENSP00000381045.2:p.Trp791Ter
ENST00000438097.2:c.2304G>A
ENSP00000411258.1:p.Trp768Ter
ENST00000428984.3:c.2304G>A
ENSP00000401265.2:p.Trp768Ter
ENST00000232165.4:c.2373G>A
ENSP00000232165.4:p.Trp791Ter
LRG_15:g.103763G>A
LRG_15t1.1:c.2304G>A
LRG_15p1.1:p.Trp768Ter

Variation displays