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.1768G>A (p.Glu590Lys)
CA10360416
680382 (ClinVar)
Gene: CDKL5
Condition: CDKL5 disorder
Inheritance Mode: X-linked inheritance
UUID: 05067df3-3a57-4067-95be-a1f6bd26509f
Approved on: 2023-03-17
Published on: 2023-03-31
HGVS expressions
NM_001323289.2:c.1768G>A
NM_001323289.2(CDKL5):c.1768G>A (p.Glu590Lys)
NC_000023.11:g.18604692G>A
CM000685.2:g.18604692G>A
NC_000023.10:g.18622812G>A
CM000685.1:g.18622812G>A
NC_000023.9:g.18532733G>A
NG_008475.1:g.184088G>A
ENST00000623535.2:c.1768G>A
ENST00000635828.1:c.1768G>A
ENST00000674046.1:c.1768G>A
ENST00000379989.6:c.1768G>A
ENST00000379996.7:c.1768G>A
ENST00000463994.4:c.1768G>A
ENST00000623535.1:n.1768G>A
NM_001037343.1:c.1768G>A
NM_003159.2:c.1768G>A
NM_001323289.1:c.1768G>A
NM_001037343.2:c.1768G>A
NM_003159.3:c.1768G>A
Evidence submitted by expert panel
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