RGD:150490255 Rat Genome Database

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Variant: RGD:150490255 -  Homo sapiens

RGD ID: 150490255
RS ID: rs2070923
ClinVar ID: CV1279575
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105371082  PRM2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 11,369,855
GRCh38 16 11,275,998
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001286359.2:c.*9+55C>A
NM_001286357.2:c.228-92C>A
NM_001286356.2:c.272-17C>A
NM_002762.4:c.272-61C>A
More... 		11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRM2
Accession:NM_001286359
Location:3UTRS;INTRON

Gene Symbol:PRM2
Accession:NM_001286356
Location:INTRON

Gene Symbol:PRM2
Accession:NM_002762
Location:INTRON

Gene Symbol:PRM2
Accession:NM_001286357
Location:INTRON

Gene Symbol:PRM2
Accession:NM_001286358
Location:INTRON

Gene Symbol:LOC105371082
Accession:XR_933073
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_933072
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_933075
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_933071
Location:INTRON;NON-CODING

Gene Symbol:PRM2
Accession:NR_104428
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_933074
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_933070
Location:INTRON;NON-CODING

Gene Symbol:LOC105371082
Accession:XR_007064985
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001716436 CLINVAR
dbSNP (RS) rs2070923 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRM2 CLINVAR
OMIM 182890 CLINVAR