RGD:405077690 Rat Genome Database

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Variant: RGD:405077690 -  Homo sapiens

RGD ID: 405077690
ClinVar ID: CV3114615
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAGLU  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 40,690,669
GRCh38 17 42,538,651
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000263.4:c.679-19C>T
NG_011552.1:g.7719C>T
NC_000017.11:g.42538651C>T
NC_000017.10:g.40690669C>T
 04/30/2023 intron variant likely benign Charcot-Marie-Tooth disease axonal type 2V; CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2V; CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2V; MPS 3B; MPS III B; Mucopoly-saccharidosis type 3B; Mucopolysaccharidosis type IIIB (Sanfilippo B); MUCOPOLYSACCHARIDOSIS, TYPE IIIB; N-acetyl-alpha-d-glucosaminidase deficiency; NAGLU DEFICIENCY; Sanfilippo syndrome B
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:NAGLU
Accession:XM_017024687
Location:5UTRS;INTRON

Gene Symbol:NAGLU
Accession:XM_047436139
Location:5UTRS;INTRON

Gene Symbol:NAGLU
Accession:NM_000263
Location:INTRON

Gene Symbol:NAGLU
Accession:XM_024450771
Location:INTRON

Gene Symbol:NAGLU
Accession:XM_047436138
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003810177 CLINVAR
MedGen C0086648 CLINVAR
NCBI Gene NAGLU CLINVAR
OMIM 252920 CLINVAR
  609701 CLINVAR
  616491 CLINVAR
SNOMED CT 59990008 CLINVAR