Annotation Detail
Information
- Associated Genes
- IL10 IL19
- Associated Variants
-
IL10 c.378+19T>C
(
ENST00000664374.2,
ENST00000659065.2,
ENST00000471071.2,
ENST00000656872.2,
ENST00000659997.3,
ENST00000659642.2,
ENST00000423557.1 )
IL10 c.378+19T>C ( ENST00000423557.1, ENST00000471071.2, ENST00000659065.2, ENST00000659642.2, ENST00000664374.2, ENST00000656872.2, ENST00000659997.3 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_153758.5(IL19):c.-339A>G AND not specified
- ClinVar Allele ID
- 1153432
- ClinVar RefSeq Alternation Syntax
- NM_153758.5:c.-339A>G
- ClinVar RefSeq Alternation Syntax
- NM_000572.3:c.378+19T>C
- ClinVar RefSeq Alternation Syntax
- NM_001393490.1:c.-149+58A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382624.1:c.123+19T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-11-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003399292
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs