Annotation Detail
Information
- Associated Genes
- COL7A1
- Associated Variants
-
COL7A1 p.Gly1595Arg (p.G1595R)
(
ENST00000328333.12,
ENST00000681320.1 )
COL7A1 p.Gly1595Arg (p.G1595R) ( ENST00000328333.12, ENST00000681320.1 ) - Associated Disease
- nonsyndromic congenital nail disorder 8
- Source Database
- ClinVar
- Description
- NM_000094.4(COL7A1):c.4783G>C (p.Gly1595Arg) AND Nonsyndromic congenital nail disorder 8
- ClinVar Allele ID
- 32482
- ClinVar RefSeq Alternation Syntax
- NM_000094.4:c.4783G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2002-02-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000022474
- ClinVar Disease
- Nonsyndromic congenital nail disorder 8
- Observed Origin Sample
- germline
- Pubmed
- 11843659
Drugs