Annotation Detail
Information
- Associated Genes
- MECP2
- Associated Variants
-
MECP2 p.Pro399Leu (p.P399L)
(
ENST00000303391.11,
ENST00000407218.5,
ENST00000415944.4,
ENST00000453960.7,
ENST00000628176.2 )
MECP2 p.Pro399Leu (p.P399L) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 ) - Associated Disease
- Rett syndrome Autism, susceptibility to, X-linked 3 syndromic X-linked intellectual disability Lubs type Severe neonatal-onset encephalopathy with microcephaly X-linked intellectual disability-psychosis-macroorchidism syndrome
- Source Database
- ClinVar
- Description
- NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu) AND multiple conditions
- ClinVar Allele ID
- 153115
- ClinVar RefSeq Alternation Syntax
- NM_001369391.2:c.881C>T
- ClinVar RefSeq Alternation Syntax
- NM_004992.4:c.1160C>T
- ClinVar RefSeq Alternation Syntax
- NM_001316337.2:c.881C>T
- ClinVar RefSeq Alternation Syntax
- NM_001369392.2:c.881C>T
- ClinVar RefSeq Alternation Syntax
- NM_001369393.2:c.881C>T
- ClinVar RefSeq Alternation Syntax
- NM_001369394.2:c.881C>T
- ClinVar RefSeq Alternation Syntax
- NM_001386138.1:c.491C>T
- ClinVar RefSeq Alternation Syntax
- NM_001386137.1:c.491C>T
- ClinVar RefSeq Alternation Syntax
- NM_001110792.2:c.1196C>T
- ClinVar RefSeq Alternation Syntax
- NM_001386139.1:c.491C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2022-01-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002498651
- ClinVar Disease
- Severe neonatal-onset encephalopathy with microcephaly
- ClinVar Disease
- Syndromic X-linked intellectual disability Lubs type
- ClinVar Disease
- Rett syndrome
- ClinVar Disease
- Autism, susceptibility to, X-linked 3
- ClinVar Disease
- X-linked intellectual disability-psychosis-macroorchidism syndrome
- Observed Origin Sample
- unknown
Drugs