Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 15:25370865 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971559

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_048_UBE3A_601623_0004, 10350

This variation has 18 HGVS names - click the plus to show

15:g.25370865G>A
ENST00000566215.3:c.1249C>T
ENSP00000457771.1:p.Arg417Ter
ENST00000397954.4:c.1318C>T
ENSP00000381045.2:p.Arg440Ter
ENST00000453082.3:n.4133-2657G>A
ENST00000614096.2:c.1309C>T
ENSP00000481796.1:p.Arg437Ter
ENST00000554726.1:n.246-20731G>A
ENST00000438097.3:c.1249C>T
ENSP00000411258.1:p.Arg417Ter
ENST00000428984.4:c.1249C>T
ENSP00000401265.2:p.Arg417Ter
ENST00000232165.5:c.1318C>T
ENSP00000232165.4:p.Arg440Ter
LRG_15:g.73117C>T
LRG_15t1:c.1249C>T
LRG_15p1:p.Arg417Ter

Variation displays