RGD:9850461 Rat Genome Database

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Variant: RGD:9850461 -  Homo sapiens

RGD ID: 9850461
RS ID: rs7601
ClinVar ID: CV167495
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRC1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 91,509,592
GRCh38 15 90,966,362
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.90966362T>C
NC_000015.9:g.91509592T>C
NM_199413.3:c.*769A>G
NM_001267580.2:c.*812A>G
More... 		02/01/2014 2kb upstream variant|3 prime utr variant uncertain significance Breast cancer, familial
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PRC1
Accession:NM_199413
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:NM_003981
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:NM_001267580
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_005254987
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_006720760
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_006720759
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522192
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522190
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522189
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522188
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522187
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_017022716
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_017022713
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_017022712
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_017022714
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433314
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433310
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433313
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433311
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433305
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433306
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433300
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433301
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433309
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433307
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433298
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433297
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433304
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433299
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_047433295
Location:3UTRS;EXON

Gene Symbol:PRC1
Accession:XM_011522191
Location:INTRON

Gene Symbol:PRC1
Accession:XM_047433308
Location:INTRON

Gene Symbol:PRC1
Accession:XM_047433303
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000162271 CLINVAR
dbSNP (RS) rs7601 CLINVAR
MedGen C0346153 CLINVAR
NCBI Gene PRC1 CLINVAR
OMIM 114480 CLINVAR
  603484 CLINVAR
SNOMED CT 254843006 CLINVAR