RGD:11660512 Rat Genome Database

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Variant: RGD:11660512 -  Homo sapiens

RGD ID: 11660512
RS ID: rs886050883
ClinVar ID: CV337724
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TDP1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 14 90,423,076
GRCh38 14 89,956,732
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009164.1:g.5831T>C
NC_000014.9:g.89956732T>C
NC_000014.8:g.90423076T>C
NM_018319.3:c.-76T>C
More...
06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TDP1
Accession:XM_047431570
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_006720197
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_047431577
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:NM_018319
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_047431576
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_047431572
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_047431568
Location:5UTRS;EXON

Gene Symbol:TDP1
Accession:XM_047431579
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_047431573
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_017021440
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:NM_001330205
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_047431569
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_005267848
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:NM_001008744
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_011536942
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XM_047431578
Location:5UTRS;INTRON

Gene Symbol:TDP1
Accession:XR_007064035
Location:EXON;NON-CODING

Gene Symbol:TDP1
Accession:XR_007064034
Location:EXON;NON-CODING

Gene Symbol:TDP1
Accession:XR_007064032
Location:EXON;NON-CODING

Gene Symbol:TDP1
Accession:XM_047431574
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431575
Location:INTRON

Gene Symbol:TDP1
Accession:XR_007064033
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000367697 CLINVAR
dbSNP (RS) rs886050883 CLINVAR
MedGen C4759870 CLINVAR
NCBI Gene TDP1 CLINVAR
OMIM 607198 CLINVAR
  607250 CLINVAR