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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Variant: NM_001323289.2(CDKL5):c.1579C>T (p.Pro527Ser)
- Curation Version - 1.0
- Curation History
- JSON LD for Version 1.0
CA412361753
590134 (ClinVar)
Gene: CDKL5
Condition: CDKL5 disorder
Inheritance Mode: X-linked inheritance
UUID: 195acd73-f998-4ce4-af7b-24705f7e18f6
Approved on: 2023-02-20
Published on: 2023-12-08
HGVS expressions
NM_001323289.2:c.1579C>T
NM_001323289.2(CDKL5):c.1579C>T (p.Pro527Ser)
NC_000023.11:g.18604503C>T
CM000685.2:g.18604503C>T
NC_000023.10:g.18622623C>T
CM000685.1:g.18622623C>T
NC_000023.9:g.18532544C>T
NG_008475.1:g.183899C>T
ENST00000623535.2:c.1579C>T
ENST00000635828.1:c.1579C>T
ENST00000674046.1:c.1579C>T
ENST00000379989.6:c.1579C>T
ENST00000379996.7:c.1579C>T
ENST00000463994.4:c.1579C>T
ENST00000623535.1:c.1579C>T
NM_001037343.1:c.1579C>T
NM_003159.2:c.1579C>T
NM_001323289.1:c.1579C>T
NM_001037343.2:c.1579C>T
NM_003159.3:c.1579C>T
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Evidence submitted by expert panel
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