RGD:150452095 Rat Genome Database

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Variant: RGD:150452095 -  Homo sapiens

RGD ID: 150452095
RS ID: rs229588
ClinVar ID: CV1220951
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SPTB  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 65,263,003
GRCh38 14 64,796,285
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1130t1:c.1341+272C>G
LRG_1130t2:c.1341+272C>G
NM_001024858.4:c.1341+272C>G
NM_001355436.2:c.1341+272C>G
More... 		11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SPTB
Accession:XM_024449699
Location:INTRON

Gene Symbol:SPTB
Accession:XM_047431724
Location:INTRON

Gene Symbol:SPTB
Accession:XM_047431725
Location:INTRON

Gene Symbol:SPTB
Accession:NM_001355436
Location:INTRON

Gene Symbol:SPTB
Accession:NM_001355437
Location:INTRON

Gene Symbol:SPTB
Accession:NM_001024858
Location:INTRON

Gene Symbol:SPTB
Accession:XM_017021612
Location:INTRON

Gene Symbol:SPTB
Accession:XM_011537105
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001612045 CLINVAR
dbSNP (RS) rs229588 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SPTB CLINVAR
OMIM 182870 CLINVAR