Annotation Detail
Information
- Associated Genes
- COL7A1
- Associated Variants
-
COL7A1 p.Pro1277Leu (p.P1277L)
(
ENST00000328333.12,
ENST00000681320.1 )
COL7A1 p.Pro1277Leu (p.P1277L) ( ENST00000328333.12, ENST00000681320.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000094.4(COL7A1):c.3830C>T (p.Pro1277Leu) AND not provided
- ClinVar Allele ID
- 251197
- ClinVar RefSeq Alternation Syntax
- NM_000094.4:c.3830C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-02-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001523645
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs