RGD:12845123 Rat Genome Database

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Variant: RGD:12845123 -  Homo sapiens

RGD ID: 12845123
RS ID: rs200874913
ClinVar ID: CV369546
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSPP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 68,026,112
GRCh38 8 67,113,877
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024790.6:c.1272+15C>T
NG_034100.1:g.54510C>T
NC_000008.11:g.67113877C>T
NC_000008.10:g.68026112C>T
More... 		10/30/2020 intron variant benign|likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CSPP1
Accession:NM_001363131
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001291339
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_011517599
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_017013854
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_005251305
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_011517598
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422244
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422246
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422251
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_006716474
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001363132
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422257
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001363133
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001382391
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422260
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422250
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_024790
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_011517611
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422254
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422255
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001364869
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422245
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422249
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422256
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422261
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422258
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422252
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422262
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_017013849
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422253
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422259
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_006716477
Location:INTRON

Gene Symbol:CSPP1
Accession:NM_001364870
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_017013847
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_047422247
Location:INTRON

Gene Symbol:CSPP1
Accession:XM_011517601
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001514360 CLINVAR
  RCV001698279 CLINVAR
dbSNP (RS) rs200874913 CLINVAR
MedGen C3661900 CLINVAR
  C3810212 CLINVAR
NCBI Gene CSPP1 CLINVAR
OMIM 611654 CLINVAR
  615636 CLINVAR