Annotation Detail
Information
- Associated Genes
- KDM6A
- Associated Variants
-
KDM6A p.Arg571Ter (p.R571*)
(
ENST00000543216.6,
ENST00000377967.9,
ENST00000382899.9,
ENST00000536777.6,
ENST00000611820.5,
ENST00000674586.1,
ENST00000674867.1,
ENST00000683021.1 )
KDM6A p.Arg571Ter (p.R571*) ( ENST00000377967.9, ENST00000382899.9, ENST00000536777.6, ENST00000543216.6, ENST00000611820.5, ENST00000674586.1, ENST00000674867.1, ENST00000683021.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_001291415.2(KDM6A):c.1711C>T (p.Arg571Ter) AND Inborn genetic diseases
- ClinVar Allele ID
- 48506
- ClinVar RefSeq Alternation Syntax
- NM_001291421.2:c.667C>T
- ClinVar RefSeq Alternation Syntax
- NM_001291416.2:c.1576C>T
- ClinVar RefSeq Alternation Syntax
- NM_001291417.2:c.1420C>T
- ClinVar RefSeq Alternation Syntax
- NM_001291415.2:c.1711C>T
- ClinVar RefSeq Alternation Syntax
- NR_111960.2:n.1838C>T
- ClinVar RefSeq Alternation Syntax
- NM_001291418.2:c.1318C>T
- ClinVar RefSeq Alternation Syntax
- NM_021140.4:c.1555C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-09-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002513317
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs