RGD:14718017 Rat Genome Database

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Variant: RGD:14718017 -  Homo sapiens

RGD ID: 14718017
RS ID: rs79397936
ClinVar ID: CV660488
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRDM5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 121,631,178
GRCh38 4 120,710,023
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001300823.2:c.1635+286G>A
NM_001379104.1:c.1761+286G>A
NG_031862.2:g.217836G>A
NC_000004.12:g.120710023C>T
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRDM5
Accession:NM_001300824
Location:3UTRS;INTRON

Gene Symbol:PRDM5
Accession:XM_011531568
Location:3UTRS;INTRON

Gene Symbol:PRDM5
Accession:XM_017007670
Location:3UTRS;INTRON

Gene Symbol:PRDM5
Accession:XM_047449559
Location:3UTRS;INTRON

Gene Symbol:PRDM5
Accession:XM_011531565
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449555
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531564
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_005262708
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001379106
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449557
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_017007671
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449558
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_017007668
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_018699
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001300823
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449556
Location:INTRON

Gene Symbol:PRDM5
Accession:NM_001379104
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531566
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_047449554
Location:INTRON

Gene Symbol:PRDM5
Accession:XM_011531563
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 RCV000830257 CLINVAR
dbSNP (RS) rs79397936 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRDM5 CLINVAR
OMIM 614161 CLINVAR