RGD:150476009 Rat Genome Database

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Variant: RGD:150476009 -  Homo sapiens

RGD ID: 150476009
RS ID: rs6451413
ClinVar ID: CV1279173
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FYB1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 39,137,380
GRCh38 5 39,137,278
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1351t1:c.1515+322T>C
LRG_1351t2:c.1545+322T>C
NM_001349333.2:c.1515+322T>C
NM_001465.6:c.1515+322T>C
More... 		06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FYB1
Accession:NM_199335
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001465
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001243093
Location:INTRON

Gene Symbol:FYB1
Accession:XM_006714464
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514011
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514010
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514008
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514009
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514012
Location:INTRON

Gene Symbol:FYB1
Accession:XM_011514013
Location:INTRON

Gene Symbol:FYB1
Accession:NM_001349333
Location:INTRON

Gene Symbol:FYB1
Accession:NM_018594
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417073
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417072
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417074
Location:INTRON

Gene Symbol:FYB1
Accession:XM_047417071
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001713922 CLINVAR
dbSNP (RS) rs6451413 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FYB1 CLINVAR
OMIM 602731 CLINVAR