Annotation Detail
Information
- Associated Genes
- CSF2RB
- Associated Variants
-
CSF2RB p.Pro702Ser (p.P702S)
(
ENST00000403662.8,
ENST00000406230.5 )
CSF2RB p.Pro702Ser (p.P702S) ( ENST00000403662.8, ENST00000406230.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000395.3(CSF2RB):c.2086C>T (p.Pro696Ser) AND not specified
- ClinVar Allele ID
- 231183
- ClinVar RefSeq Alternation Syntax
- NM_000395.3:c.2086C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2014-11-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000216230
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs