rs145960760 Rat Genome Database

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Variant: rs145960760 -  Homo sapiens

RGD ID: 11634104
RS ID: rs145960760
ClinVar ID: CV297586
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CBR4  PALLD  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 169,849,545
GRCh38 4 168,928,394
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_013376.1:g.436329C>T
NC_000004.12:g.168928394C>T
NC_000004.11:g.169849545C>T
NM_001166109.2:c.*2009C>T
More... 		01/13/2018 3 prime utr variant benign|likely benign adult 1-9 / 1 000 000 Pancreatic cancer 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PALLD
Accession:XM_011531772
Location:3UTRS;EXON

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

Gene Symbol:PALLD
Accession:XM_024453939
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_047449868
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_047449865
Location:3UTRS;EXON

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

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

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

Gene Symbol:CBR4
Accession:XM_017008783
Location:3UTRS;EXON

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

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

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

Gene Symbol:PALLD
Accession:XM_047449866
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:XM_047449864
Location:3UTRS;EXON

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

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

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

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

Gene Symbol:CBR4
Accession:XM_047416331
Location:3UTRS;EXON

Gene Symbol:PALLD
Accession:XM_047449862
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532386
Location:INTRON

Gene Symbol:CBR4
Accession:NM_032783
Location:INTRON

Gene Symbol:CBR4
Accession:XM_017008782
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449870
Location:INTRON

Gene Symbol:CBR4
Accession:XM_005263315
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449869
Location:INTRON

Gene Symbol:CBR4
Accession:XM_006714391
Location:INTRON

Gene Symbol:CBR4
Accession:XM_011532385
Location:INTRON

Gene Symbol:PALLD
Accession:XM_047449861
Location:INTRON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000396315 CLINVAR
dbSNP (RS) rs145960760 CLINVAR
MedGen C1847351 CLINVAR
NCBI Gene CBR4 CLINVAR
  PALLD CLINVAR
OMIM 606856 CLINVAR
  608092 CLINVAR
  619394 CLINVAR