Transcript #00000293

Transcript name SCO cytochrome oxidase deficient homolog 2 (yeast), transcript variant 4
Gene name SCO2 (SCO2 cytochrome c oxidase assembly protein)
Chromosome 22
Transcript - NCBI ID NM_001169111.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001162582.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

84 entries on 1 page. Showing entries 1 - 84.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-1011T>C p.(=) - - - -
./. - - c.-1005C>T p.(=) - - - -
./. - - c.-982C>T p.(=) - - - -
./. - - c.-967_-958delinsAA p.(=) - - - -
./. - - c.-966_-965insGCGGCGCTGGACGACGGC p.(=) - - - -
./. - - c.-949T>G p.(=) - - - -
./. - - c.-933G>A p.(=) - - - -
./. - - c.-910T>C p.(=) - - - -
./. - - c.-889del p.(=) - - - -
./. - - c.-865T>C p.(=) - - - -
./. - - c.-840G>A p.(=) - - - -
./. - - c.-830G>A p.(=) - - - -
./. - - c.-818G>A p.(=) - - - -
./. - - c.-816T>A p.(=) - - - -
./. - - c.-813G>A p.(=) - - - -
./. - - c.-715A>C p.(=) - - - -
./. - - c.-715A>G p.(=) - - - -
./. - - c.-714G>A p.(=) - - - -
./. - - c.-714G>C p.(=) - - - -
./. - - c.-713G>A p.(=) - - - -
./. - - c.-697C>T p.(=) - - - -
./. - - c.-680_-675del p.(=) - - - -
./. - - c.-662_-661insT p.(=) - - - -
./. - - c.-591G>A p.(=) - - - -
./. - - c.-589T>A p.(=) - - - -
./. - - c.-572G>A p.(=) - - - -
./. - - c.-571T>A p.(=) - - - -
./. - - c.-491G>A p.(=) - - - -
./. - - c.-483_-482insC p.(=) - - - -
./. - - c.-480del p.(=) - - - -
./. - - c.-480G>A p.(=) - - - -
./. - - c.-471_-470insG p.(=) - - - -
./. - - c.-464_-445del p.(=) - - - -
./. - - c.-440_-439insC p.(=) - - - -
./. - - c.-431G>C p.(=) - - - -
./. - - c.-398G>A p.(=) - - - -
./. - - c.-396_-391del p.(=) - - - -
./. - - c.-390C>T p.(=) - - - -
./. - - c.-381_-380insC p.(=) - - - -
./. - - c.-379C>A p.(=) - - - -
./. - - c.-379C>T p.(=) - - - -
./. - - c.-360_-359insT p.(=) - - - -
./. - - c.-359C>T p.(=) - - - -
./. - - c.-350C>T p.(=) - - - -
./. - - c.-348G>A p.(=) - - - -
./. - - c.-339C>T p.(=) - - - -
./. - - c.-332G>A p.(=) - - - -
./. - - c.-313G>A p.(=) - - - -
./. - - c.-172G>C p.(=) - - - -
./. - - c.-162_-161insCTGC p.(=) - - - -
./. - - c.-144G>C p.(=) - - - -
./. - - c.-113A>G p.(=) - - - -
./. - - c.-108G>C p.(=) - - - -
./. - - c.-81C>T p.(=) - - - -
./. - - c.-48G>A p.(=) - - - -
./. - - c.4C>G p.(Leu2Val) - - - -
./. - - c.59G>C p.(Arg20Pro) - - - -
+/+ - 2/2 c.107G>A p.(Trp36*) - stop_gained - -
./. - 2/2 c.107G>A p.(Trp36*) - stop_gained - -
./. - - c.107G>A p.(Trp36*) - - - -
./. - - 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) - - - -
./. - - c.398G>A p.(Cys133Tyr) - - - -
./. - 2/2 c.398G>A p.(Cys133Tyr) probably_damaging(1) missense_variant - deleterious(0)
./. - 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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