Annotation Detail
Information
- Associated Genes
- FECH
- Associated Variants
-
FECH c.1095+1G>A
(
ENST00000262093.11,
ENST00000382873.8,
ENST00000652755.1 )
FECH c.1095+1G>A ( ENST00000262093.11, ENST00000382873.8, ENST00000652755.1 ) - Associated Disease
- Protoporphyria, erythropoietic, 1
- Source Database
- ClinVar
- Description
- NM_000140.5(FECH):c.1077+1G>A AND Protoporphyria, erythropoietic, 1
- ClinVar Allele ID
- 15591
- ClinVar RefSeq Alternation Syntax
- NM_001371094.1:c.978+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001371095.1:c.861+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001012515.4:c.1095+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_000140.5:c.1077+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001374778.1:c.1077+1G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1993-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000000582
- ClinVar Disease
- Protoporphyria, erythropoietic, 1
- Observed Origin Sample
- germline
- Pubmed
- 8500787
- Pubmed
- 3940245
Drugs