RGD:150461375 Rat Genome Database

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Variant: RGD:150461375 -  Homo sapiens

RGD ID: 150461375
RS ID: rs12754483
ClinVar ID: CV1215797
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NTNG1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 107,937,468
GRCh38 1 107,394,846
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001113226.3:c.888-308C>G
NM_001372167.1:c.888-308C>G
NM_001372168.1:c.888-308C>G
NM_001372170.1:c.888-308C>G
More... 		06/20/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NTNG1
Accession:NM_001113228
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001113226
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_014917
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_011541025
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001312688
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_017000683
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_017000686
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001330665
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372167
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372169
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372166
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372168
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372170
Location:INTRON

Gene Symbol:NTNG1
Accession:NM_001372171
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_047449449
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_047449447
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_047449448
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_047449446
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001613500 CLINVAR
dbSNP (RS) rs12754483 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NTNG1 CLINVAR
OMIM 608818 CLINVAR