RGD:150461927 Rat Genome Database

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Variant: RGD:150461927 -  Homo sapiens

RGD ID: 150461927
RS ID: rs202201074
ClinVar ID: CV1206520
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CIB2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 78,397,719
GRCh38 15 78,105,377
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.78105377G>A
NC_000015.9:g.78397719G>A
NM_001271889.2:c.396-45C>T
NM_001271888.2:c.414-45C>T
More... 		12/05/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CIB2
Accession:XM_005254126
Location:3UTRS;EXON

Gene Symbol:CIB2
Accession:XM_011521161
Location:3UTRS;EXON

Gene Symbol:CIB2
Accession:NM_006383
Location:INTRON

Gene Symbol:CIB2
Accession:NM_001271889
Location:INTRON

Gene Symbol:CIB2
Accession:NM_001271888
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 RCV001586921 CLINVAR
dbSNP (RS) rs202201074 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CIB2 CLINVAR
OMIM 605564 CLINVAR