RGD:150460891 Rat Genome Database

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Variant: RGD:150460891 -  Homo sapiens

RGD ID: 150460891
RS ID: rs1952979
ClinVar ID: CV1231406
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDC5L  POLR1C  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 44,374,508
GRCh38 6 44,406,771
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001253.4:c.903+304G>A
NM_001318876.2:c.946-35119G>A
NC_000006.12:g.44406771G>A
NG_028283.4:g.894684G>A
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:POLR1C
Accession:XM_047419577
Location:INTRON

Gene Symbol:CDC5L
Accession:XM_047419605
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_203290
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_001363658
Location:INTRON

Gene Symbol:CDC5L
Accession:NM_001253
Location:INTRON

Gene Symbol:POLR1C
Accession:NM_001318876
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001640971 CLINVAR
dbSNP (RS) rs1952979 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDC5L CLINVAR
  POLR1C CLINVAR
OMIM 602868 CLINVAR
  610060 CLINVAR