Original source

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

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

Chromosome 15:25616872 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041096

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_051_UBE3A_601623_0007, 10353

This variation has 15 HGVS names - click the plus to show

15:g.25616872A>G
ENST00000554726.1:n.246-19871A>G
ENST00000566215.1:c.389T>C
ENSP00000457771.1:p.Ile130Thr
ENST00000397954.2:c.458T>C
ENSP00000381045.2:p.Ile153Thr
ENST00000438097.1:c.389T>C
ENSP00000411258.1:p.Ile130Thr
ENST00000232165.3:c.449T>C
ENSP00000232165.3:p.Ile150Thr
ENST00000428984.2:c.389T>C
ENSP00000401265.2:p.Ile130Thr
LRG_15:g.72257T>C
LRG_15t1.1:c.389T>C
LRG_15p1.1:p.Ile130Thr

Variation displays