rs1553986519 Rat Genome Database

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Variant: rs1553986519 -  Homo sapiens

RGD ID: 11633012
RS ID: rs1553986519
ClinVar ID: CV294120
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: CBR4  PALLD  
Reference Nucleotide: -
Variant Nucleotide: ATT
Position
Assembly Chr Position
GRCh37 4 169,849,117
GRCh38 4 168,927,966
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Age of Onset
Prevalence
Trait Synonyms
NG_013376.1:g.435901_435902insATT
NC_000004.12:g.168927966_168927967insATT
NC_000004.11:g.169849117_169849118insATT
NM_001166109.2:c.*1581_*1582insATT
More... 		06/14/2016 3 prime utr variant uncertain significance adult 1-9 / 1 000 000 Exocrine pancreatic carcinoma; PANCREATIC ACINAR CARCINOMA; Pancreatic cancer, somatic; PANCREATIC CARCINOMA; Pancreatic carcinoma, somatic
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV294120Humanpancreatic carcinoma  IAGP 8554872ClinVar Annotator: match by term: Carcinoma of pancreasClinVar 
Gene Symbol:PALLD
Accession:XM_024453939
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_024453940
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449865
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449864
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531774
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001367567
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001367569
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449868
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_016081
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531772
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001166109
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001166108
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001166110
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531768
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001367570
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531773
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:NM_001367568
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449867
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531769
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449863
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531771
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_011531775
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449866
Location:3UTRS;EXON

Gene Symbol:CBR4
Accession:XM_017008783
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449861
Location:INTRON

Gene Symbol:CBR4
Accession:XM_006714391
Location:INTRON

Gene Symbol:CBR4
Accession:NM_032783
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532386
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449862
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449870
Location:INTRON

Gene Symbol:CBR4
Accession:XM_017008782
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449869
Location:INTRON

Gene Symbol:CBR4
Accession:XM_047416331
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532385
Location:INTRON

Gene Symbol:CBR4
Accession:XM_005263315
Location:INTRON

Gene Symbol:CBR4
Accession:XR_007057980
Location:INTRON;NON-CODING

Gene Symbol:CBR4
Accession:XR_001741341
Location:INTRON;NON-CODING

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1 to 9 of 9 rows
Database
Acc Id
Source(s)
ClinVar RCV000303576 CLINVAR
dbSNP (RS) rs1553986519 CLINVAR
MedGen C0235974 CLINVAR
NCBI Gene CBR4 CLINVAR
  PALLD CLINVAR
OMIM 260350 CLINVAR
  608092 CLINVAR
  619394 CLINVAR
SNOMED CT 372142002 CLINVAR
1 to 9 of 9 rows