Annotation Detail
Information
- Associated Genes
- KRT5
- Associated Variants
-
KRT5 p.Pro25Leu (p.P25L)
(
ENST00000252242.9 )
KRT5 p.Pro25Leu (p.P25L) ( ENST00000252242.9 ) - Associated Disease
- epidermolysis bullosa simplex with mottled pigmentation
- Source Database
- ClinVar
- Description
- NM_000424.4(KRT5):c.74C>T (p.Pro25Leu) AND Epidermolysis bullosa simplex with mottled pigmentation
- ClinVar Allele ID
- 29687
- ClinVar RefSeq Alternation Syntax
- NM_000424.4:c.74C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2010-11-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000015754
- ClinVar Disease
- Epidermolysis bullosa simplex with mottled pigmentation
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
- Pubmed
- 2476664
- Pubmed
- 8799157
- Pubmed
- 6457621
- Pubmed
- 20923750
- Pubmed
- 11167681
- Pubmed
- 10494094
- Pubmed
- 421361
- Pubmed
- 9129237
- Pubmed
- 16581562
Drugs