RGD:156323847 Rat Genome Database

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Variant: RGD:156323847 -  Homo sapiens

RGD ID: 156323847
ClinVar ID: CV1890884
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM216  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 61,165,729
GRCh38 11 61,398,257
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_698t1:c.432-4A>G
LRG_698t2:c.432-13A>G
NM_001330285.2:c.249-13A>G
NM_016499.6:c.249-4A>G
More... 		09/02/2022 intron variant likely benign Cerebelloparenchymal disorder 4; CEREBELLOPARENCHYMAL DISORDER IV; Joubert syndrome; Joubert-Boltshauser syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TMEM216
Accession:NM_001173991
Location:INTRON

Gene Symbol:TMEM216
Accession:NM_001330285
Location:INTRON

Gene Symbol:TMEM216
Accession:NM_016499
Location:INTRON

Gene Symbol:TMEM216
Accession:NM_001173990
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003089351 CLINVAR
MedGen C0431399 CLINVAR
NCBI Gene TMEM216 CLINVAR
OMIM 213300 CLINVAR
  613277 CLINVAR
SNOMED CT 253175003 CLINVAR