Transcript #00000076

Transcript name COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast)
Gene name COX10 (cytochrome c oxidase assembly homolog 10 (yeast))
Chromosome 17
Transcript - NCBI ID NM_001303.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001294.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-170C>G p.(=) - - - -
./. - - c.-112G>A p.(=) - - - -
./. - - c.-109G>A p.(=) - - - -
./. - - c.-90G>T p.(=) - - - -
./. - - c.-63C>T p.(=) - - - -
./. - - c.-40G>A p.(=) - - - -
./. - - c.-29C>A p.(=) - - - -
./. - - c.-24G>A p.(=) - - - -
./. - - c.2T>C p.? - - - -
./. - - c.33C>T p.(=) - - - -
./. - - c.64T>A p.(Trp22Arg) - - - -
./. - - c.83C>T p.(Thr28Ile) - - - -
./. - - c.123G>A p.(=) - - - -
./. - - c.173G>A p.(Arg58His) - - - -
./. - - c.184A>T p.(Thr62Ser) - - - -
./. - - c.192G>A p.(=) - - - -
./. - - c.290A>G p.(Tyr97Cys) - - - -
./. - - c.311C>T p.(Pro104Leu) - - - -
./. - - c.476G>A p.(Arg159Gln) - - - -
./. - - c.504G>A p.(=) - - - -
./. - - c.543G>A p.(=) - - - -
./. - - c.587C>A p.(Thr196Lys) - - - -
+/+ - 4/7 c.587C>A p.(Thr196Lys) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.612C>A p.(Asn204Lys) - - - -
+/+ - 4/7 c.612C>A p.(Asn204Lys) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.624+4A>G p.? - - - -
./. - - c.674C>T p.(Pro225Leu) - - - -
+/+ - 5/7 c.674C>T p.(Pro225Leu) probably_damaging(0.998) missense_variant - tolerated(0.68)
./. - - c.699A>G p.(=) - - - -
./. - - c.909C>T p.(=) - - - -
./. - - c.928+12G>A p.(=) - - - -
./. - - c.929-12_929-11insCCC p.(=) - - - -
./. - - c.929-7C>T p.(=) - - - -
./. - - c.981C>T p.(=) - - - -
./. - - c.982G>A p.(Ala328Thr) - - - -
+/+ - 7/7 c.1007A>G p.(Asp336Gly) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.1007A>G p.(Asp336Gly) - - - -
./. - - c.1007A>T p.(Asp336Val) - - - -
+/+ - 7/7 c.1007A>T p.(Asp336Val) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.1027T>C p.(Cys343Arg) - - - -
./. - - c.1038G>A p.(=) - - - -
./. - - c.1061G>A p.(Arg354Gln) - - - -
./. - - c.*13G>A p.(=) - - - -
./. - - c.*139_*140del p.(=) - - - -
./. - - c.*139_*141del p.(=) - - - -
./. - - c.*152T>A p.(=) - - - -
./. - - c.*297G>A p.(=) - - - -
./. - - c.*322T>C p.(=) - - - -
./. - - c.*371A>G p.(=) - - - -
./. - - c.*408G>A p.(=) - - - -
./. - - c.*438G>C p.(=) - - - -
./. - - c.*535C>A p.(=) - - - -
./. - - c.*563_*564insG p.(=) - - - -
./. - - c.*591_*592del p.(=) - - - -
./. - - c.*628C>G p.(=) - - - -
./. - - c.*646C>A p.(=) - - - -
./. - - c.*646C>G p.(=) - - - -
./. - - c.*739A>G p.(=) - - - -
./. - - c.*757T>C p.(=) - - - -
./. - - c.*823C>T p.(=) - - - -
./. - - c.*831_*832del p.(=) - - - -
./. - - c.*974C>A p.(=) - - - -
./. - - c.*1076T>C p.(=) - - - -
./. - - c.*1078C>T p.(=) - - - -
./. - - c.*1101C>T p.(=) - - - -
./. - - c.*1324C>T p.(=) - - - -
./. - - c.*1367G>A p.(=) - - - -
./. - - c.*1385C>T p.(=) - - - -
./. - - c.*1459del p.(=) - - - -
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