RGD:150442180 Rat Genome Database

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Variant: RGD:150442180 -  Homo sapiens

RGD ID: 150442180
RS ID: rs74867614
ClinVar ID: CV1204665
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CIB2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 78,415,796
GRCh38 15 78,123,454
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001271888.2:c.-44+7711C>T
NM_001271889.2:c.51+7711C>T
NM_001301224.2:c.86+251C>T
NM_006383.4:c.86+251C>T
More... 		12/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CIB2
Accession:NM_001271888
Location:5UTRS;INTRON

Gene Symbol:CIB2
Accession:XM_011521161
Location:5UTRS;INTRON

Gene Symbol:CIB2
Accession:NM_006383
Location:INTRON

Gene Symbol:CIB2
Accession:NM_001271889
Location:INTRON

Gene Symbol:CIB2
Accession:XM_005254126
Location:INTRON

Gene Symbol:CIB2
Accession:NM_001301224
Location:INTRON

Gene Symbol:CIB2
Accession:XM_047432110
Location:INTRON

Gene Symbol:CIB2
Accession:NR_125435
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001583772 CLINVAR
dbSNP (RS) rs74867614 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CIB2 CLINVAR
OMIM 605564 CLINVAR