RGD:150454773 Rat Genome Database

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Variant: RGD:150454773 -  Homo sapiens

RGD ID: 150454773
RS ID: rs4915045
ClinVar ID: CV1266069
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NTNG1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 108,023,589
GRCh38 1 107,480,967
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.*127A>C
NM_001113228.3:c.*127A>C
NM_001312688.2:c.*127A>C
NM_001330665.2:c.*127A>C
More... 		06/20/2021 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NTNG1
Accession:NM_001113228
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001113226
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_014917
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001312688
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_017000683
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001330665
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372167
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372169
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372166
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372168
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372170
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:NM_001372171
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_047449449
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_047449447
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_047449448
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_047449446
Location:3UTRS;EXON

Gene Symbol:NTNG1
Accession:XM_011541025
Location:INTRON

Gene Symbol:NTNG1
Accession:XM_017000686
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001692646 CLINVAR
dbSNP (RS) rs4915045 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NTNG1 CLINVAR
OMIM 608818 CLINVAR