Annotation Detail
Information
- Associated Genes
- FCRL3
- Associated Variants
-
FCRL3 p.Asn721Ser (p.N721S)
(
ENST00000368184.8,
ENST00000368186.9 )
FCRL3 p.Asn721Ser (p.N721S) ( ENST00000368184.8, ENST00000368186.9 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_052939.4(FCRL3):c.2162A>G (p.Asn721Ser) AND not provided
- ClinVar Allele ID
- 1281484
- ClinVar RefSeq Alternation Syntax
- NM_052939.4:c.2162A>G
- ClinVar RefSeq Alternation Syntax
- NR_135214.2:n.2384A>G
- ClinVar RefSeq Alternation Syntax
- NR_135217.2:n.2081A>G
- ClinVar RefSeq Alternation Syntax
- NM_001320333.2:c.2162A>G
- ClinVar RefSeq Alternation Syntax
- NR_135215.2:n.2366A>G
- ClinVar RefSeq Alternation Syntax
- NR_135216.2:n.2271A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-02-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001716897
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs