Annotation Detail
Information
- Associated Genes
- SHOX
- Associated Variants
-
SHOX p.Tyr199Ter (p.Y199*)
(
ENST00000334060.8,
ENST00000381575.6,
ENST00000381578.6,
ENST00000686671.1 )
SHOX p.Tyr199Ter (p.Y199*) ( ENST00000711141.1, ENST00000711142.1, ENST00000711143.1, ENST00000711145.1 )
SHOX p.Tyr199Ter (p.Y199*) ( ENST00000334060.8, ENST00000381575.6, ENST00000381578.6, ENST00000686671.1 )
SHOX p.Tyr199Ter (p.Y199*) ( ENST00000711141.1, ENST00000711142.1, ENST00000711143.1, ENST00000711145.1 ) - Associated Disease
- Leri-Weill dyschondrosteosis
- Source Database
- ClinVar
- Description
- NM_000451.4(SHOX):c.597C>G (p.Tyr199Ter) AND Leri-Weill dyschondrosteosis
- ClinVar Allele ID
- 24912
- ClinVar RefSeq Alternation Syntax
- NM_000451.4:c.597C>G
- ClinVar RefSeq Alternation Syntax
- NM_006883.2:c.597C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1998-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000010548
- ClinVar Disease
- Leri-Weill dyschondrosteosis
- Observed Origin Sample
- germline
- Pubmed
- 9590293
Drugs