RGD:15146858 Rat Genome Database

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Variant: RGD:15146858 -  Homo sapiens

RGD ID: 15146858
RS ID: rs377104007
ClinVar ID: CV775659
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ITGB1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 33,199,141
GRCh38 10 32,910,213
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_133376.3:c.2164+10C>T
NM_002211.4:c.2164+10C>T
NM_033668.2:c.2164+10C>T
NG_029012.1:g.53153C>T
More... 		12/28/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ITGB1
Accession:NM_033668
Location:INTRON

Gene Symbol:ITGB1
Accession:NM_133376
Location:INTRON

Gene Symbol:ITGB1
Accession:NM_002211
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000944812 CLINVAR
dbSNP (RS) rs377104007 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ITGB1 CLINVAR
OMIM 135630 CLINVAR