Annotation Detail
Information
- Associated Genes
- MTHFR
- Associated Variants
-
MTHFR p.Ser481= (p.S481=)
(
ENST00000376585.6,
ENST00000376583.7,
ENST00000423400.7,
ENST00000641820.1,
ENST00000376590.9,
ENST00000376592.6,
ENST00000641407.1 )
MTHFR p.Ser481= (p.S481=) ( ENST00000376583.7, ENST00000376585.6, ENST00000376590.9, ENST00000376592.6, ENST00000423400.7, ENST00000641407.1, ENST00000641820.1 ) - Associated Disease
- thrombophilia due to thrombin defect schizophrenia Homocystinuria due to methylene tetrahydrofolate reductase deficiency Neural tube defects, folate-sensitive
- Source Database
- ClinVar
- Description
- NM_005957.5(MTHFR):c.1320G>A (p.Ser440=) AND multiple conditions
- ClinVar Allele ID
- 185770
- ClinVar RefSeq Alternation Syntax
- NM_001330358.2:c.1443G>A
- ClinVar RefSeq Alternation Syntax
- NM_005957.5:c.1320G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2021-08-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002498831
- ClinVar Disease
- Thrombophilia due to thrombin defect
- ClinVar Disease
- Homocystinuria due to methylene tetrahydrofolate reductase deficiency
- ClinVar Disease
- Neural tube defects, folate-sensitive
- ClinVar Disease
- Schizophrenia
- Observed Origin Sample
- unknown
Drugs