RGD:15098623 Rat Genome Database

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Variant: RGD:15098623 -  Homo sapiens

RGD ID: 15098623
RS ID: rs141414113
ClinVar ID: CV730747
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRDM10  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 129,812,530
GRCh38 11 129,942,635
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367895.1:c.-87-6G>A
NM_001367896.1:c.-87-6G>A
NM_001367897.1:c.-87-6G>A
NM_001367898.1:c.505-6G>A
More... 		07/06/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRDM10
Accession:NM_001367897
Location:5UTRS;INTRON

Gene Symbol:PRDM10
Accession:NM_001367895
Location:5UTRS;INTRON

Gene Symbol:PRDM10
Accession:NM_001367896
Location:5UTRS;INTRON

Gene Symbol:PRDM10
Accession:NM_199437
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367898
Location:INTRON

Gene Symbol:PRDM10
Accession:XM_047427311
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_199439
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367894
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367890
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367899
Location:INTRON

Gene Symbol:PRDM10
Accession:XM_047427312
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_020228
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_199438
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367893
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367891
Location:INTRON

Gene Symbol:PRDM10
Accession:XM_011542912
Location:INTRON

Gene Symbol:PRDM10
Accession:NM_001367892
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000891780 CLINVAR
dbSNP (RS) rs141414113 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRDM10 CLINVAR
OMIM 618319 CLINVAR