Annotation Detail
Information
- Associated Genes
- MEFV
- Associated Variants
-
MEFV p.Arg408Gln (p.R408Q)
(
ENST00000536379.5,
ENST00000339854.8,
ENST00000219596.6,
ENST00000541159.5 )
MEFV p.Arg408Gln (p.R408Q) ( ENST00000219596.6, ENST00000339854.8, ENST00000536379.5, ENST00000541159.5 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000243.3(MEFV):c.1223G>A (p.Arg408Gln) AND Inborn genetic diseases
- ClinVar Allele ID
- 17591
- ClinVar RefSeq Alternation Syntax
- NM_000243.3:c.1223G>A
- ClinVar RefSeq Alternation Syntax
- NM_001198536.2:c.590G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2017-03-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002362552
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs