RGD:150499762 Rat Genome Database

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Variant: RGD:150499762 -  Homo sapiens

RGD ID: 150499762
RS ID: rs41302832
ClinVar ID: CV1224650
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FYB1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 39,153,529
GRCh38 5 39,153,427
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1351t1:c.1292+21C>T
LRG_1351t2:c.1322+21C>T
NM_001349333.2:c.1292+21C>T
NM_199335.5:c.1292+21C>T
More... 		11/11/2018 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 RCV001620481 CLINVAR
dbSNP (RS) rs41302832 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FYB1 CLINVAR
OMIM 602731 CLINVAR