rs886059212 Rat Genome Database

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Variant: rs886059212 -  Homo sapiens

RGD ID: 11650464
RS ID: rs886059212
ClinVar ID: CV297571
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CBR4  PALLD  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 169,848,239
GRCh38 4 168,927,088
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.435023A>G
NC_000004.12:g.168927088A>G
NC_000004.11:g.169848239A>G
NM_001166109.2:c.*703A>G
More... 		01/12/2018 3 prime utr variant uncertain significance adult 1-9 / 1 000 000 Pancreatic cancer 1
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV297571Humanpancreatic cancer  IAGP 8554872ClinVar Annotator: match by term: PANCREATIC CANCER more ...ClinVar 
Gene Symbol:PALLD
Accession:XM_047449864
Location:3UTRS;EXON

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

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

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

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

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

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

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

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

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

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

Gene Symbol:PALLD
Accession:XM_024453939
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_047449866
Location:3UTRS;EXON

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

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

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

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

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

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

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

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

Gene Symbol:CBR4
Accession:XM_047416331
Location:INTRON

Gene Symbol:CBR4
Accession:XM_005263315
Location:INTRON

Gene Symbol:CBR4
Accession:XM_017008782
Location:INTRON

Gene Symbol:CBR4
Accession:XM_017008783
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532386
Location:INTRON

Gene Symbol:CBR4
Accession:XM_006714391
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449869
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449870
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532385
Location:INTRON

Gene Symbol:CBR4
Accession:NM_032783
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449862
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449861
Location:INTRON

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

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

.


Database
Acc Id
Source(s)
ClinVar RCV000293190 CLINVAR
dbSNP (RS) rs886059212 CLINVAR
MedGen C1847351 CLINVAR
NCBI Gene CBR4 CLINVAR
  PALLD CLINVAR
OMIM 606856 CLINVAR
  608092 CLINVAR
  619394 CLINVAR