Transcript #00000290

Transcript name SCO cytochrome oxidase deficient homolog 2 (yeast), transcript variant 2
Gene name SCO2 (SCO2 cytochrome c oxidase assembly protein)
Chromosome 22
Transcript - NCBI ID NM_001169109.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001162580.1
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.-207T>C p.(=) - - - -
./. - - c.-201C>T p.(=) - - - -
./. - - c.-178C>T p.(=) - - - -
./. - - c.-163_-154delinsAA p.(=) - - - -
./. - - c.-162_-161insGCGGCGCTGGACGACGGC p.(=) - - - -
./. - - c.-145T>G p.(=) - - - -
./. - - c.-129G>A p.(=) - - - -
./. - - c.-106T>C p.(=) - - - -
./. - - c.-85del p.(=) - - - -
./. - - c.-61T>C p.(=) - - - -
./. - - c.-36G>A p.(=) - - - -
./. - - c.-26G>A p.(=) - - - -
./. - - c.-14G>A p.(=) - - - -
./. - - c.-14+2T>A p.? - - - -
./. - - c.-14+5G>A p.? - - - -
./. - - c.-14+103A>C p.(=) - - - -
./. - - c.-14+103A>G p.(=) - - - -
./. - - c.-14+104G>A p.(=) - - - -
./. - - c.-14+104G>C p.(=) - - - -
./. - - c.-14+105G>A p.(=) - - - -
./. - - c.-14+121C>T p.(=) - - - -
./. - - c.-14+138_-14+143del p.(=) - - - -
./. - - c.-14+156_-14+157insT p.(=) - - - -
./. - - c.-14+227G>A p.(=) - - - -
./. - - c.-14+229T>A p.(=) - - - -
./. - - c.-14+246G>A p.(=) - - - -
./. - - c.-14+247T>A p.(=) - - - -
./. - - c.-14+327G>A p.(=) - - - -
./. - - c.-14+335_-14+336insC p.(=) - - - -
./. - - c.-14+338del p.(=) - - - -
./. - - c.-14+338G>A p.(=) - - - -
./. - - c.-14+347_-14+348insG p.(=) - - - -
./. - - c.-14+354_-14+373del p.(=) - - - -
./. - - c.-14+378_-14+379insC p.(=) - - - -
./. - - c.-14+387G>C p.(=) - - - -
./. - - c.-14+420G>A p.(=) - - - -
./. - - c.-14+422_-14+427del p.(=) - - - -
./. - - c.-14+428C>T p.(=) - - - -
./. - - c.-14+437_-14+438insC p.(=) - - - -
./. - - c.-14+439C>A p.(=) - - - -
./. - - c.-14+439C>T p.(=) - - - -
./. - - c.-14+458_-14+459insT p.(=) - - - -
./. - - c.-14+459C>T p.(=) - - - -
./. - - c.-14+468C>T p.(=) - - - -
./. - - c.-14+470G>A p.(=) - - - -
./. - - c.-14+479C>T p.(=) - - - -
./. - - c.-14+486G>A p.(=) - - - -
./. - - c.-14+505G>A p.(=) - - - -
./. - - c.-14+646G>C p.(=) - - - -
./. - - c.-14+656_-14+657insCTGC p.(=) - - - -
./. - - c.-14+674G>C p.(=) - - - -
./. - - c.-14+705A>G p.(=) - - - -
./. - - c.-14+710G>C p.(=) - - - -
./. - - c.-14+737C>T p.(=) - - - -
./. - - c.-14+770G>A p.(=) - - - -
./. - - c.4C>G p.(Leu2Val) - - - -
./. - - c.59G>C p.(Arg20Pro) - - - -
./. - - c.107G>A p.(Trp36*) - - - -
+/+ - 2/2 c.107G>A p.(Trp36*) - stop_gained - -
./. - 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) - - - -
./. - - c.418G>A p.(Glu140Lys) - - - -
./. - 2/2 c.418G>A p.(Glu140Lys) probably_damaging(1) missense_variant - deleterious(0)
./. - 2/2 c.511C>T p.(Arg171Trp) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.511C>T p.(Arg171Trp) - - - -
./. - - 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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