RGD:11615026 Rat Genome Database

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Variant: RGD:11615026 -  Homo sapiens

RGD ID: 11615026
RS ID: rs370991229
ClinVar ID: CV330987
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TDP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 90,446,981
GRCh38 14 89,980,637
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.29736G>A
NC_000014.9:g.89980637G>A
NC_000014.8:g.90446981G>A
NM_001330205.2:c.884+5G>A
More...
06/14/2016 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:TDP1
Accession:NM_018319
Location:INTRON

Gene Symbol:TDP1
Accession:NM_001008744
Location:INTRON

Gene Symbol:TDP1
Accession:XM_005267848
Location:INTRON

Gene Symbol:TDP1
Accession:XM_006720197
Location:INTRON

Gene Symbol:TDP1
Accession:XM_011536942
Location:INTRON

Gene Symbol:TDP1
Accession:XM_017021440
Location:INTRON

Gene Symbol:TDP1
Accession:NM_001330205
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431570
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431568
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431576
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431569
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431577
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431573
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431572
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431579
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431578
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431574
Location:INTRON

Gene Symbol:TDP1
Accession:XM_047431575
Location:INTRON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000281726 CLINVAR
dbSNP (RS) rs370991229 CLINVAR
MedGen C4759870 CLINVAR
NCBI Gene TDP1 CLINVAR
OMIM 607198 CLINVAR
  607250 CLINVAR