Transcript #00000291

Transcript name SCO cytochrome oxidase deficient homolog 2 (yeast), transcript variant 3
Gene name SCO2 (SCO2 cytochrome c oxidase assembly protein)
Chromosome 22
Transcript - NCBI ID NM_001169110.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001162581.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

84 entries on 1 page. Showing entries 1 - 84.
Legend  

Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-452T>C p.(=) - - - -
./. - - c.-446C>T p.(=) - - - -
./. - - c.-423C>T p.(=) - - - -
./. - - c.-408_-399delinsAA p.(=) - - - -
./. - - c.-407_-406insGCGGCGCTGGACGACGGC p.(=) - - - -
./. - - c.-390T>G p.(=) - - - -
./. - - c.-374G>A p.(=) - - - -
./. - - c.-351T>C p.(=) - - - -
./. - - c.-330del p.(=) - - - -
./. - - c.-306T>C p.(=) - - - -
./. - - c.-281G>A p.(=) - - - -
./. - - c.-271G>A p.(=) - - - -
./. - - c.-259G>A p.(=) - - - -
./. - - c.-257T>A p.(=) - - - -
./. - - c.-254G>A p.(=) - - - -
./. - - c.-156A>C p.(=) - - - -
./. - - c.-156A>G p.(=) - - - -
./. - - c.-155G>A p.(=) - - - -
./. - - c.-155G>C p.(=) - - - -
./. - - c.-154G>A p.(=) - - - -
./. - - c.-138C>T p.(=) - - - -
./. - - c.-121_-116del p.(=) - - - -
./. - - c.-103_-102insT p.(=) - - - -
./. - - c.-32G>A p.(=) - - - -
./. - - c.-30T>A p.(=) - - - -
./. - - c.-14+1G>A p.? - - - -
./. - - c.-14+2T>A p.? - - - -
./. - - c.-14+82G>A p.(=) - - - -
./. - - c.-14+90_-14+91insC p.(=) - - - -
./. - - c.-14+93del p.(=) - - - -
./. - - c.-14+93G>A p.(=) - - - -
./. - - c.-14+102_-14+103insG p.(=) - - - -
./. - - c.-14+109_-14+128del p.(=) - - - -
./. - - c.-14+133_-14+134insC p.(=) - - - -
./. - - c.-14+142G>C p.(=) - - - -
./. - - c.-14+175G>A p.(=) - - - -
./. - - c.-14+177_-14+182del p.(=) - - - -
./. - - c.-14+183C>T p.(=) - - - -
./. - - c.-14+192_-14+193insC p.(=) - - - -
./. - - c.-14+194C>A p.(=) - - - -
./. - - c.-14+194C>T p.(=) - - - -
./. - - c.-14+213_-14+214insT p.(=) - - - -
./. - - c.-14+214C>T p.(=) - - - -
./. - - c.-14+223C>T p.(=) - - - -
./. - - c.-14+225G>A p.(=) - - - -
./. - - c.-14+234C>T p.(=) - - - -
./. - - c.-14+241G>A p.(=) - - - -
./. - - c.-14+260G>A p.(=) - - - -
./. - - c.-14+401G>C p.(=) - - - -
./. - - c.-14+411_-14+412insCTGC p.(=) - - - -
./. - - c.-14+429G>C p.(=) - - - -
./. - - c.-14+460A>G p.(=) - - - -
./. - - c.-14+465G>C p.(=) - - - -
./. - - c.-14+492C>T p.(=) - - - -
./. - - c.-14+525G>A p.(=) - - - -
./. - - c.4C>G p.(Leu2Val) - - - -
./. - - c.59G>C p.(Arg20Pro) - - - -
./. - 2/2 c.107G>A p.(Trp36*) - stop_gained - -
./. - - c.107G>A p.(Trp36*) - - - -
+/+ - 2/2 c.107G>A p.(Trp36*) - stop_gained - -
./. - - c.157C>T p.(Gln53*) - - - -
./. - 2/2 c.157C>T p.(Gln53*) - stop_gained - -
./. - - c.162C>T p.(=) - - - -
./. - - c.201C>T p.(=) - - - -
./. - - c.237G>A p.(=) - - - -
./. - - c.244A>G p.(Lys82Glu) - - - -
./. - 2/2 c.268C>T p.(Arg90*) - stop_gained - -
./. - - c.268C>T p.(Arg90*) - - - -
./. - - c.276A>G p.(=) - - - -
./. - - c.327C>T p.(=) - - - -
./. - - c.378G>A p.(Met126Ile) - - - -
./. - 2/2 c.398G>A p.(Cys133Tyr) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.398G>A p.(Cys133Tyr) - - - -
./. - 2/2 c.418G>A p.(Glu140Lys) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.418G>A p.(Glu140Lys) - - - -
./. - - c.511C>T p.(Arg171Trp) - - - -
./. - 2/2 c.511C>T p.(Arg171Trp) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.582C>T p.(=) - - - -
./. - - c.633A>C p.(=) - - - -
./. - 2/2 c.674C>T p.(Ser225Phe) probably_damaging(0.992) missense_variant - deleterious(0)
./. - - c.674C>T p.(Ser225Phe) - - - -
./. - - c.738G>C p.(=) - - - -
./. - - c.763C>A p.(=) - - - -
./. - - c.776C>T p.(Ala259Val) - - - -
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