Annotation Detail
Information
- Associated Genes
- GLB1
- Associated Variants
-
GLB1 p.Pro429Ser (p.P429S)
(
ENST00000307363.10,
ENST00000307377.12,
ENST00000399402.7 )
GLB1 p.Pro366His (p.P366H) ( ENST00000307363.10, ENST00000307377.12, ENST00000399402.7 )
GLB1 p.Pro429Ser (p.P429S) ( ENST00000307363.10, ENST00000307377.12, ENST00000399402.7 )
GLB1 p.Pro366His (p.P366H) ( ENST00000307363.10, ENST00000307377.12, ENST00000399402.7 ) - Associated Disease
- Mucopolysaccharidosis, MPS-IV-B
- Source Database
- ClinVar
- Description
- NM_000404.2(GLB1):c.[1285C>T;1097C>A] AND Mucopolysaccharidosis, MPS-IV-B
- ClinVar Allele ID
- 205011
- ClinVar Allele ID
- 205010
- ClinVar RefSeq Alternation Syntax
- NM_001135602.3:c.892C>T
- ClinVar RefSeq Alternation Syntax
- NM_001079811.3:c.1007C>A
- ClinVar RefSeq Alternation Syntax
- NM_000404.4:c.1285C>T
- ClinVar RefSeq Alternation Syntax
- NM_001135602.3:c.704C>A
- ClinVar RefSeq Alternation Syntax
- NM_001317040.2:c.1429C>T
- ClinVar RefSeq Alternation Syntax
- NM_001317040.2:c.1241C>A
- ClinVar RefSeq Alternation Syntax
- NM_001393580.1:c.1285C>T
- ClinVar RefSeq Alternation Syntax
- NM_001079811.3:c.1195C>T
- ClinVar RefSeq Alternation Syntax
- NM_001393580.1:c.1097C>A
- ClinVar RefSeq Alternation Syntax
- NM_000404.4:c.1097C>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2016-05-13
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000190508
- ClinVar Disease
- Mucopolysaccharidosis, MPS-IV-B
- Observed Origin Sample
- germline
Drugs