RGD:11596108 Rat Genome Database

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Variant: RGD:11596108 -  Homo sapiens

RGD ID: 11596108
RS ID: rs539733007
ClinVar ID: CV303446
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD36  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 80,231,670
GRCh38 7 80,602,354
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001289911.2:c.-134C>T
NM_001001547.3:c.-209C>T
NG_008192.1:g.5167C>T
NC_000007.14:g.80602354C>T
More...
06/14/2016 5 prime utr variant uncertain significance CD36 DEFICIENCY; Platelet glycoprotein IV deficiency
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CD36
Accession:XM_024447003
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001371081
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001289911
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001371075
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001371074
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001001547
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001371080
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421049
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421047
Location:INTRON

Gene Symbol:CD36
Accession:NM_001127444
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421043
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421045
Location:INTRON

Gene Symbol:CD36
Accession:NM_001127443
Location:INTRON

Gene Symbol:CD36
Accession:NM_001289909
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421044
Location:INTRON

Gene Symbol:CD36
Accession:NM_000072
Location:INTRON

Gene Symbol:CD36
Accession:NM_001001548
Location:INTRON

Gene Symbol:CD36
Accession:NM_001371077
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421046
Location:INTRON

Gene Symbol:CD36
Accession:XM_005250715
Location:INTRON

Gene Symbol:CD36
Accession:NM_001371079
Location:INTRON

Gene Symbol:CD36
Accession:XM_024447002
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421048
Location:INTRON

Gene Symbol:CD36
Accession:NM_001289908
Location:INTRON

Gene Symbol:CD36
Accession:NM_001371078
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421041
Location:INTRON

Gene Symbol:CD36
Accession:XM_047421042
Location:INTRON

Gene Symbol:CD36
Accession:NR_110501
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000378420 CLINVAR
dbSNP (RS) rs539733007 CLINVAR
MedGen C1842090 CLINVAR
NCBI Gene CD36 CLINVAR
OMIM 173510 CLINVAR
  608404 CLINVAR