Transcript #00009332 (NM_000072.3, CD36 gene)

Transcript name transcript variant 3
Gene name CD36 (CD36 molecule (thrombospondin receptor))
Chromosome 7
Transcript - NCBI ID NM_000072.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000063.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:35:09 +01:00 (CET)
Date last edited N/A


Variants

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.121-6T>C 121 r.(=) p.(=) - splice 6
./. - c.158A>G 158 r.(?) p.(Asn53Ser) - missense -
./. - c.158A>G 158 r.(?) p.(Asn53Ser) - missense -
./. - c.158A>G 158 r.(?) p.(Asn53Ser) - missense -
./. - c.158A>G 158 r.(?) p.(Asn53Ser) - missense -
./. - c.268C>T 268 r.(?) p.(Pro90Ser) - missense -
./. - c.282-31T>C 282 r.(=) p.(=) - intron 31
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.282-10A>G 282 r.(=) p.(=) - intron 10
./. - c.429+35A>C 429 r.(=) p.(=) - intron 35
./. - c.573G>A 573 r.(?) p.(=) - coding-synonymous -
./. - c.748+24A>G 748 r.(=) p.(=) - intron 24
./. - c.879T>C 879 r.(?) p.(=) - coding-synonymous -
./. - c.975T>G 975 r.(?) p.(Tyr325Ter) - stop-gained -
./. - c.975T>G 975 r.(?) p.(Tyr325Ter) - stop-gained -
./. - c.975T>G 975 r.(?) p.(Tyr325Ter) - stop-gained -
./. - c.975T>G 975 r.(?) p.(Tyr325Ter) - stop-gained -
./. - c.1007-24T>C 1007 r.(=) p.(=) - intron 24
./. - c.1125+13C>A 1125 r.(=) p.(=) - intron 13
./. - c.1125+13C>A 1125 r.(=) p.(=) - intron 13
./. - c.1125+13C>A 1125 r.(=) p.(=) - intron 13
./. - c.1163A>T 1163 r.(?) p.(Gln388Leu) - missense -
./. - c.1199+37G>A 1199 r.(=) p.(=) - intron 37
./. - c.1199+37G>A 1199 r.(=) p.(=) - intron 37
./. - c.1417_*1del 1417 r.(=) p.(=) - codingComplex -
./. - c.1417_*1del 1417 r.(=) p.(=) - codingComplex -
./. - c.1417_*1del 1417 r.(=) p.(=) - codingComplex -
./. - c.1417_*1del 1417 r.(=) p.(=) - codingComplex -
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