Annotation Detail
Information
- Associated Genes
- ANO5
- Associated Variants
-
ANO5 c.762+1G>A
(
ENST00000324559.9,
ENST00000683197.1,
ENST00000682266.1,
ENST00000683437.1,
ENST00000682341.1,
ENST00000683411.1,
ENST00000684663.1 )
ANO5 c.762+1G>A ( ENST00000324559.9, ENST00000682266.1, ENST00000682341.1, ENST00000683197.1, ENST00000683411.1, ENST00000683437.1, ENST00000684663.1 ) - Associated Disease
- autosomal recessive limb-girdle muscular dystrophy type 2L
- Source Database
- ClinVar
- Description
- NM_213599.3(ANO5):c.762+1G>A AND Autosomal recessive limb-girdle muscular dystrophy type 2L
- ClinVar Allele ID
- 213817
- ClinVar RefSeq Alternation Syntax
- NM_001410964.1:c.717+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_213599.3:c.762+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142649.2:c.759+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001410963.1:c.720+1G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2014-06-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000201014
- ClinVar Disease
- Autosomal recessive limb-girdle muscular dystrophy type 2L
- Observed Origin Sample
- germline
Drugs