RGD:151858823 Rat Genome Database

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Variant: RGD:151858823 -  Homo sapiens

RGD ID: 151858823
RS ID: rs1037433593
ClinVar ID: CV1389485
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CFB  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 31,917,930
GRCh38 6 31,950,153
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_136:g.9210C>T
NG_008191.1:g.9210C>T
NC_000006.12:g.31950153C>T
NC_000006.11:g.31917930C>T
More...
07/04/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CFB
Accession:NM_001710
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001905024 CLINVAR
dbSNP (RS) rs1037433593 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CFB CLINVAR
OMIM 138470 CLINVAR