RGD:25329368 Rat Genome Database

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Variant: RGD:25329368 -  Homo sapiens

RGD ID: 25329368
RS ID: rs1580455560
ClinVar ID: CV807837
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APC  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 112,137,079
GRCh38 5 112,801,382
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354906.2:c.-203A>C
NM_001354900.2:c.656A>C
NM_001354901.2:c.656A>C
NM_001354905.2:c.656A>C
More... 		12/26/2018 5 prime utr variant uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:APC
Accession:NM_001354906
Location:5UTRS;EXON

Gene Symbol:APC
Accession:NM_001407470
Location:5UTRS;EXON

Gene Symbol:APC
Accession:NM_001407472
Location:5UTRS;EXON

Gene Symbol:APC
Accession:NM_001407471
Location:5UTRS;EXON

Gene Symbol:APC
Accession:NM_001127511
Location:EXON

Gene Symbol:APC
Accession:NM_001127510
Location:EXON

Gene Symbol:APC
Accession:NM_000038
Location:EXON

Gene Symbol:APC
Accession:NM_001354895
Location:EXON

Gene Symbol:APC
Accession:NM_001354897
Location:EXON

Gene Symbol:APC
Accession:NM_001354902
Location:EXON

Gene Symbol:APC
Accession:NM_001354898
Location:EXON

Gene Symbol:APC
Accession:NM_001354904
Location:EXON

Gene Symbol:APC
Accession:NM_001354896
Location:EXON

Gene Symbol:APC
Accession:NM_001354903
Location:EXON

Gene Symbol:APC
Accession:NM_001354899
Location:EXON

Gene Symbol:APC
Accession:NM_001354900
Location:EXON

Gene Symbol:APC
Accession:NM_001354901
Location:EXON

Gene Symbol:APC
Accession:NM_001354905
Location:EXON

Gene Symbol:APC
Accession:NM_001407447
Location:EXON

Gene Symbol:APC
Accession:NM_001407456
Location:EXON

Gene Symbol:APC
Accession:NM_001407460
Location:EXON

Gene Symbol:APC
Accession:NM_001407452
Location:EXON

Gene Symbol:APC
Accession:NM_001407469
Location:EXON

Gene Symbol:APC
Accession:NM_001407446
Location:EXON

Gene Symbol:APC
Accession:NM_001407448
Location:EXON

Gene Symbol:APC
Accession:NM_001407450
Location:EXON

Gene Symbol:APC
Accession:NM_001407457
Location:EXON

Gene Symbol:APC
Accession:NM_001407458
Location:EXON

Gene Symbol:APC
Accession:NM_001407453
Location:EXON

Gene Symbol:APC
Accession:NM_001407449
Location:EXON

Gene Symbol:APC
Accession:NM_001407455
Location:EXON

Gene Symbol:APC
Accession:NM_001407459
Location:EXON

Gene Symbol:APC
Accession:NM_001407451
Location:EXON

Gene Symbol:APC
Accession:NM_001407454
Location:EXON

Gene Symbol:APC
Accession:NM_001407467
Location:EXON

Gene Symbol:APC
Accession:NR_176366
Location:EXON;NON-CODING

Gene Symbol:APC
Accession:NR_176365
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001017581 CLINVAR
dbSNP (RS) rs1580455560 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene APC CLINVAR
OMIM 611731 CLINVAR
SNOMED CT 699346009 CLINVAR