Transcript #00000082

Transcript name transcript variant X1
Gene name COX15 (cytochrome c oxidase assembly homolog 15 (yeast))
Chromosome 10
Transcript - NCBI ID XM_005269539.1
Transcript - Ensembl ID -
Protein - NCBI ID XP_005269596.1
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.-602C>A p.(=) - - - -
./. - - c.-597A>C p.(=) - - - -
./. - - c.-472T>C p.(=) - - - -
./. - - c.-435C>T p.(=) - - - -
./. - - c.-406C>G p.(=) - - - -
./. - - c.-398C>A p.(=) - - - -
./. - - c.-338C>T p.(=) - - - -
./. - - c.-307C>G p.(=) - - - -
./. - - c.-232C>T p.(=) - - - -
./. - - c.-133T>C p.(=) - - - -
./. - - c.-114A>G p.(=) - - - -
./. - - c.-84G>A p.? - - - -
./. - - c.-71T>C p.(=) - - - -
./. - - c.-26A>G p.(=) - - - -
./. - - c.107G>A p.(Arg36His) - - - -
./. - - c.131G>A p.(Ser44Asn) - - - -
./. - - c.161G>A p.(Gly54Glu) - - - -
./. - - c.164G>A p.(Arg55Lys) - - - -
./. - - c.255T>C p.(=) - - - -
./. - - c.396-3C>G p.? - - - -
./. - - c.406G>C p.(Asp136His) - - - -
./. - - c.452C>G p.(Ser151*) - - - -
./. - - c.532C>T p.(Arg178Cys) - - - -
./. - - c.582+14A>G p.(=) - - - -
+/+ - 5/9 c.649C>T p.(Arg217Trp) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.649C>T p.(Arg217Trp) - - - -
./. - - c.717G>T p.(Trp239Cys) - - - -
./. - - c.784C>T p.(Arg262*) - - - -
./. - - c.929C>G p.(Pro310Arg) - - - -
./. - - c.988-3C>T p.? - - - -
./. - - c.1029C>A p.(=) - - - -
./. - - c.1030T>C p.(Ser344Pro) - - - -
./. - - c.1101+2883C>G p.(=) - - - -
./. - - c.1101+2887T>C p.(=) - - - -
./. - - c.1101+2958T>C p.(=) - - - -
./. - - c.1101+3070T>C p.(=) - - - -
./. - - c.1101+3122C>T p.(=) - - - -
./. - - c.1101+3190_1101+3191del p.(=) - - - -
./. - - c.1101+3235C>T p.(=) - - - -
./. - - c.1101+3355C>G p.(=) - - - -
./. - - c.1101+3454G>A p.(=) - - - -
./. - - c.1101+3477G>A p.(=) - - - -
./. - - c.1101+3537T>A p.(=) - - - -
./. - - c.1101+3554G>A p.(=) - - - -
./. - - c.1101+3611G>T p.(=) - - - -
./. - - c.1101+3612G>T p.(=) - - - -
./. - - c.1101+3821C>T p.(=) - - - -
./. - - c.1101+3954A>T p.(=) - - - -
./. - - c.1101+4043G>A p.(=) - - - -
./. - - c.1101+4220G>T p.(=) - - - -
./. - - c.1101+4251T>C p.(=) - - - -
./. - - c.1101+4410G>A p.(=) - - - -
./. - - c.1101+4429C>G p.(=) - - - -
./. - - c.1101+4462A>G p.(=) - - - -
./. - - c.1101+4516del p.(=) - - - -
./. - - c.1101+4618A>G p.(=) - - - -
./. - - c.1101+4659A>G p.(=) - - - -
./. - - c.1101+5008T>C p.(=) - - - -
./. - - c.1101+5178T>C p.(=) - - - -
./. - - c.1101+5246_1101+5247insT p.(=) - - - -
./. - - c.1101+5246_1101+5247insTT p.(=) - - - -
./. - - c.1101+5431G>A p.(=) - - - -
./. - - c.1101+5574T>G p.(=) - - - -
./. - - c.1101+5676A>G p.(=) - - - -
./. - - c.1101+5775G>A p.(=) - - - -
./. - - c.1101+5776T>C p.(=) - - - -
./. - - c.1101+6020G>T p.(=) - - - -
./. - - c.1101+6144C>T p.(=) - - - -
./. - - c.1101+6202A>C p.(=) - - - -
./. - - c.1101+6264A>G p.(=) - - - -
./. - - c.1101+6500C>T p.(=) - - - -
./. - - c.1101+6581A>T p.(=) - - - -
./. - - c.1101+6595T>C p.(=) - - - -
./. - - c.1101+6663C>G p.(=) - - - -
./. - - c.1101+6689G>A p.(=) - - - -
./. - - c.1101+6751A>G p.(=) - - - -
./. - - c.1101+7044T>G p.(=) - - - -
./. - - c.1101+7086C>T p.(=) - - - -
./. - - c.1101+7152C>T p.(=) - - - -
./. - - c.1101+7326G>A p.(=) - - - -
./. - - c.1101+7369A>G p.(=) - - - -
./. - - c.1101+7373G>A p.(=) - - - -
./. - - c.1101+7375G>C p.(=) - - - -
./. - - c.1101+7407T>C p.(=) - - - -
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