RGD:150499435 Rat Genome Database

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Variant: RGD:150499435 -  Homo sapiens

RGD ID: 150499435
RS ID: rs2808470
ClinVar ID: CV1254358
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C4BPA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 207,287,187
GRCh38 1 207,113,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_547t1:c.143-258C>T
NM_000715.4:c.143-258C>T
LRG_547:g.14581C>T
NG_029579.1:g.14581C>T
More... 		06/18/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:C4BPA
Accession:NM_000715
Location:INTRON

Gene Symbol:C4BPA
Accession:XM_005273251
Location:INTRON

Gene Symbol:C4BPA
Accession:XM_005273252
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676532 CLINVAR
dbSNP (RS) rs2808470 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C4BPA CLINVAR
OMIM 120830 CLINVAR