Annotation Detail

Information
Associated Genes
ARSA
Associated Variants
ARSA p.Leu300Ser (p.L300S) ( ENST00000395621.7, ENST00000453344.6, ENST00000395619.3, ENST00000216124.10, ENST00000356098.9 )
ARSA p.Leu300Ser (p.L300S) ( ENST00000453344.6, ENST00000356098.9, ENST00000395619.3, ENST00000216124.10, ENST00000395621.7 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000487.6(ARSA):c.899T>C (p.Leu300Ser) AND not provided
ClinVar Allele ID
79048
ClinVar RefSeq Alternation Syntax
NM_001085426.3:c.899T>C
ClinVar RefSeq Alternation Syntax
NM_001362782.2:c.641T>C
ClinVar RefSeq Alternation Syntax
NM_001085425.3:c.899T>C
ClinVar RefSeq Alternation Syntax
NM_000487.6:c.899T>C
ClinVar RefSeq Alternation Syntax
NM_001085427.3:c.899T>C
ClinVar RefSeq Alternation Syntax
NM_001085428.3:c.641T>C
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2012-11-14
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000058988
ClinVar Disease
not provided
Observed Origin Sample
germline
Observed Origin Sample
not provided
Drugs