Annotation Detail
Information
- Associated Genes
- MEFV
- Associated Variants
-
MEFV p.Arg408Gln (p.R408Q)
(
ENST00000536379.5,
ENST00000339854.8,
ENST00000219596.6,
ENST00000541159.5 )
MEFV p.Pro369Ser (p.P369S) ( ENST00000219596.6, ENST00000541159.5, ENST00000339854.8, ENST00000536379.5 )
MEFV p.Arg408Gln (p.R408Q) ( ENST00000219596.6, ENST00000339854.8, ENST00000536379.5, ENST00000541159.5 )
MEFV p.Pro369Ser (p.P369S) ( ENST00000219596.6, ENST00000339854.8, ENST00000536379.5, ENST00000541159.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000243.2(MEFV):c.[1105C>T;1223G>A] AND not specified
- ClinVar Allele ID
- 17590
- ClinVar Allele ID
- 17591
- ClinVar RefSeq Alternation Syntax
- NM_000243.3:c.1223G>A
- ClinVar RefSeq Alternation Syntax
- NM_001198536.2:c.472C>T
- ClinVar RefSeq Alternation Syntax
- NM_001198536.2:c.590G>A
- ClinVar RefSeq Alternation Syntax
- NM_000243.3:c.1105C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-03-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001251298
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs