RGD:150469995 Rat Genome Database

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Variant: RGD:150469995 -  Homo sapiens

RGD ID: 150469995
RS ID: rs343190
ClinVar ID: CV1247914
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRDM5  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 121,739,832
GRCh38 4 120,818,677
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018699.4:c.476-150A>C
NC_000004.11:g.121739832T>G
NM_001300823.2:c.476-150A>C
NM_001300824.2:c.476-150A>C
More... 		06/26/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRDM5
Accession:NM_001379104
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531563
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001300824
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001300823
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_017007671
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449557
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449558
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449555
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001379106
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_005262708
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_017007668
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531564
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531568
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_017007670
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449556
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531566
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_018699
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449554
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449559
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531565
Location:INTRON

Gene Symbol:PRDM5
Accession:XR_938680
Location:INTRON;NON-CODING

Gene Symbol:PRDM5
Accession:XR_938678
Location:INTRON;NON-CODING

Gene Symbol:PRDM5
Accession:XR_938679
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001670950 CLINVAR
dbSNP (RS) rs343190 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRDM5 CLINVAR
OMIM 614161 CLINVAR