The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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- See Evidence submitted by expert panel for details.
Variant: NM_130838.1(UBE3A):c.876G>A (p.Lys292=)
- Curation Version - 1.0
- Curation History
- JSON LD for Version 1.0
CA267785638
437192 (ClinVar)
Gene: UBE3A
Condition: Angelman syndrome
Inheritance Mode: Autosomal dominant inheritance (with paternal imprinting (HP:0012274))
UUID: 7be1b922-205f-47f4-9346-b5504cf92ce9
Approved on: 2021-04-02
Published on: 2021-05-10
HGVS expressions
NM_130838.1:c.876G>A
NM_130838.1(UBE3A):c.876G>A (p.Lys292=)
ENST00000438097.6:c.876G>A
ENST00000625778.3:c.876G>A
ENST00000635914.1:c.876G>A
ENST00000637886.1:c.936G>A
ENST00000638011.1:c.876G>A
ENST00000638155.1:c.876G>A
ENST00000648336.2:c.936G>A
ENST00000649550.1:c.876G>A
ENST00000650110.1:c.945G>A
ENST00000675000.1:n.1611G>A
ENST00000675177.1:c.759G>A
ENST00000675593.1:n.3632G>A
ENST00000232165.7:c.876G>A
ENST00000397954.6:c.945G>A
ENST00000428984.6:c.876G>A
ENST00000438097.5:c.876G>A
ENST00000566215.5:c.876G>A
ENST00000614096.4:c.936G>A
ENST00000625778.2:c.876G>A
ENST00000630424.2:c.876G>A
NM_000462.3:c.945G>A
NM_130839.2:c.936G>A
NM_000462.5:c.945G>A
NM_001354505.1:c.936G>A
NM_001354506.1:c.876G>A
NM_001354507.1:c.876G>A
NM_001354508.1:c.876G>A
NM_001354509.1:c.876G>A
NM_001354511.1:c.876G>A
NM_001354512.1:c.876G>A
NM_001354513.1:c.876G>A
NM_001354523.1:c.876G>A
NM_001354526.1:c.876G>A
NM_001354538.1:c.936G>A
NM_001354539.1:c.876G>A
NM_001354540.1:c.876G>A
NM_001354541.1:c.876G>A
NM_001354542.1:c.876G>A
NM_001354543.1:c.876G>A
NM_001354544.1:c.876G>A
NM_001354545.1:c.936G>A
NM_001354546.1:c.759G>A
NM_001354547.1:c.876G>A
NM_001354548.1:c.876G>A
NM_001354549.1:c.876G>A
NM_001354550.1:c.361+4227G>A
NM_001354551.1:c.301+4227G>A
NM_130838.3:c.876G>A
NM_130839.4:c.936G>A
NR_146177.1:n.18393-20358C>T
NR_148916.1:n.1484G>A
NM_001354506.2:c.876G>A
NM_001354507.2:c.876G>A
NM_001354508.2:c.876G>A
NM_001354509.2:c.876G>A
NM_001354511.2:c.876G>A
NM_001354512.2:c.876G>A
NM_001354513.2:c.876G>A
NM_001354523.2:c.876G>A
NM_001354538.2:c.936G>A
NM_001354539.2:c.876G>A
NM_001354540.2:c.876G>A
NM_001354541.2:c.876G>A
NM_001354542.2:c.876G>A
NM_001354543.2:c.876G>A
NM_001354544.2:c.876G>A
NM_001354545.2:c.936G>A
NM_001354546.2:c.759G>A
NM_001354547.2:c.876G>A
NM_001354548.2:c.876G>A
NM_001354549.2:c.876G>A
NM_001354550.2:c.361+4227G>A
NM_001354551.2:c.301+4227G>A
NM_001374461.1:c.876G>A
NM_130838.4:c.876G>A
NM_130839.5:c.936G>A
NR_148916.2:n.1452G>A
NC_000015.10:g.25371238C>T
CM000677.2:g.25371238C>T
NC_000015.9:g.25616385C>T
CM000677.1:g.25616385C>T
NC_000015.8:g.23167478C>T
NG_009268.1:g.72744G>A
Evidence submitted by expert panel
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