RGD:405199001 Rat Genome Database

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Variant: RGD:405199001 -  Homo sapiens

RGD ID: 405199001
ClinVar ID: CV3132229
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDIN1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 36,936,541
GRCh38 15 36,644,340
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321756.2:c.-147-883T>A
NM_001290232.2:c.-148+17T>A
NM_032499.6:c.-148+17T>A
NM_001321757.2:c.-257+17T>A
More... 		11/20/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CDIN1
Accession:NM_032499
Location:5UTRS;INTRON

Gene Symbol:CDIN1
Accession:NM_001290232
Location:5UTRS;INTRON

Gene Symbol:CDIN1
Accession:NM_001321757
Location:5UTRS;INTRON

Gene Symbol:CDIN1
Accession:NM_001321756
Location:5UTRS;INTRON

Gene Symbol:CDIN1
Accession:XM_047433174
Location:5UTRS;INTRON

Gene Symbol:CDIN1
Accession:NM_001130010
Location:INTRON

Gene Symbol:CDIN1
Accession:NM_001290233
Location:INTRON

Gene Symbol:CDIN1
Accession:NM_001321761
Location:INTRON

Gene Symbol:CDIN1
Accession:NM_001321759
Location:INTRON

Gene Symbol:CDIN1
Accession:NM_001321760
Location:INTRON

Gene Symbol:CDIN1
Accession:NM_001321758
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_017022676
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_017022677
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433171
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433172
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433173
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433175
Location:INTRON

Gene Symbol:CDIN1
Accession:XM_047433176
Location:INTRON

Gene Symbol:CDIN1
Accession:XR_007064491
Location:INTRON;NON-CODING

Gene Symbol:CDIN1
Accession:XR_007064492
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003821822 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDIN1 CLINVAR
OMIM 615626 CLINVAR