RGD:11601220 Rat Genome Database

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Variant: RGD:11601220 -  Homo sapiens

RGD ID: 11601220
RS ID: rs768286621
ClinVar ID: CV311772
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD36  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 80,276,030
GRCh38 7 80,646,714
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008192.1:g.49527C>T
NC_000007.14:g.80646714C>T
NC_000007.13:g.80276030C>T
NR_110501.1:n.153C>T
More...
01/12/2018 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:NM_001371079
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421047
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001371078
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421043
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001127443
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421041
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421049
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421048
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_005250715
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001289909
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_024447002
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421044
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001289908
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421046
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001001547
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_001371077
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001001548
Location:5UTRS;EXON

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

Gene Symbol:CD36
Accession:XM_047421045
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_000072
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:NM_001127444
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_024447003
Location:5UTRS;EXON

Gene Symbol:CD36
Accession:XM_047421042
Location:5UTRS;EXON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000280652 CLINVAR
dbSNP (RS) rs768286621 CLINVAR
MedGen C1842090 CLINVAR
NCBI Gene CD36 CLINVAR
OMIM 173510 CLINVAR
  608404 CLINVAR