Transcript #00000409

Transcript name transcript variant X7
Gene name ADCK3 (aarF domain containing kinase 3)
Chromosome 1
Transcript - NCBI ID XM_005273207.1
Transcript - Ensembl ID -
Protein - NCBI ID XP_005273264.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

107 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-310C>A p.(=) - - - -
./. - - c.-286A>G p.(=) - - - -
./. - - c.-248C>T p.(=) - - - -
./. - - c.-183+8T>C p.(=) - - - -
./. - - c.-182-16001G>A p.(=) - - - -
./. - - c.-182-15947G>A p.(=) - - - -
./. - - c.-182-12407G>A p.(=) - - - -
./. - - c.-182-12389C>T p.(=) - - - -
./. - - c.-182-12372T>G p.(=) - - - -
./. - - c.-182-12369A>C p.(=) - - - -
./. - - c.-182-12336C>T p.(=) - - - -
./. - - c.-182-12269G>A p.(=) - - - -
./. - - c.-182-12200G>A p.(=) - - - -
./. - - c.-182-12127_-182-12106delinsTTG p.(=) - - - -
./. - - c.-182-12106C>A p.(=) - - - -
./. - - c.-182-11734_-182-11727del p.(=) - - - -
./. - - c.-182-11730C>T p.(=) - - - -
+/+ - - c.-182-11730C>T p.(=) - - - -
./. - - c.-151G>A p.(=) - - - -
./. - - c.-141G>A p.(=) - - - -
./. - - c.-119A>C p.(=) - - - -
./. - - c.-40G>A p.(=) - - - -
./. - - c.-27C>T p.(=) - - - -
./. - - c.-23G>A p.(=) - - - -
+/+ - - c.-23G>A p.(=) - - - -
./. - - c.-23G>T p.(=) - - - -
+/+ - - c.-23G>T p.(=) - - - -
./. - - c.-8T>C p.(=) - - - -
./. - - c.58C>T p.(Arg20Trp) - - - -
./. - - c.64C>T p.(Arg22Trp) - - - -
./. - - c.156C>T p.(=) - - - -
+/+ - 5/12 c.156C>T p.(=) - synonymous_variant - -
./. - - c.163C>T p.(Arg55Trp) - - - -
./. - - c.169del p.(Phe57Serfs*14) - - - -
./. - - c.205C>T p.(Arg69*) - - - -
./. - - c.216C>T p.(=) - - - -
./. - - c.223G>A p.(Glu75Lys) - - - -
./. - - c.244-3_244-2insAGT p.? - - - -
./. - - c.299T>A p.(Leu100*) - - - -
./. - - c.326-10C>T p.(=) - - - -
./. - - c.348C>T p.(=) - - - -
./. - - c.351C>T p.(=) - - - -
./. - - c.392G>A p.(Arg131Gln) - - - -
./. - - c.419+11C>G p.(=) - - - -
./. - - c.421G>A p.(Asp141Asn) - - - -
./. - - c.449A>G p.(Tyr150Cys) - - - -
./. - - c.495_496del p.(Thr166Argfs*52) - - - -
./. - - c.559del p.(Glu187Argfs*11) - - - -
./. - - c.561+2T>C p.? - - - -
./. - - c.561+12C>A p.(=) - - - -
./. - - c.562-13G>A p.(=) - - - -
./. - - c.603C>T p.(=) - - - -
./. - - c.669+1G>A p.? - - - -
./. - - c.686T>C p.(Phe229Ser) - - - -
./. - - c.695C>T p.(Thr232Met) - - - -
+/+ - 10/12 c.704A>G p.(Tyr235Cys) probably_damaging(0.978) missense_variant - deleterious(0)
./. - - c.704A>G p.(Tyr235Cys) - - - -
./. - - c.736-20C>G p.(=) - - - -
./. - - c.807C>T p.(=) - - - -
./. - - c.808G>A p.(Gly270Ser) - - - -
+/+ - 11/12 c.808G>A p.(Gly270Ser) probably_damaging(0.991) missense_variant - deleterious(0)
+/+ - 11/12 c.814G>A p.(Glu272Lys) probably_damaging(0.996) missense_variant - deleterious(0)
./. - - c.814G>A p.(Glu272Lys) - - - -
./. - - c.823-9T>C p.(=) - - - -
./. - - c.828G>A p.(Met276Ile) - - - -
./. - - c.842T>C p.(Leu281Ser) - - - -
./. - - c.874G>A p.(Ala292Thr) - - - -
./. - - c.876C>A p.(=) - - - -
./. - - c.879T>C p.(=) - - - -
./. - - c.904_905insA p.(Ser303Glufs*148) - - - -
./. - - c.909_911del p.(Thr305del) - - - -
?/? - - c.910_912del p.(Thr305del) - - - -
?/? - - c.913_915del p.(Thr305del) - - - -
./. - - c.963C>T p.(=) - - - -
./. - - c.972C>T p.(=) - - - -
./. - - c.974_975insG p.(Glu326Glyfs*125) - - - -
?/? - 12/12 c.974_975insG p.(Glu326Glyfs*125) - frameshift_variant - -
?/? - - c.976dup p.(Glu326Glyfs*125) - - - -
./. - 12/12 c.976_977insGA p.(Glu326Glyfs*20) - frameshift_variant - -
./. - - c.1001_1002insG p.(Ser337Leufs*114) - - - -
./. - - c.1007G>A p.(Gly336Asp) - - - -
./. - - c.1028_1029insGCT p.(Leu344dup) - - - -
./. - - c.1077C>T p.(=) - - - -
./. - - c.1102C>T p.(Gln368*) - - - -
./. - - c.1105T>G p.(*369Gluext*27) - - - -
./. - - c.*22C>T p.(=) - - - -
./. - - c.*70_*71insG p.(=) - - - -
./. - - c.*133G>A p.(=) - - - -
./. - - c.*150C>T p.(=) - - - -
./. - - c.*184G>C p.(=) - - - -
./. - - c.*230G>A p.(=) - - - -
./. - - c.*252A>C p.(=) - - - -
./. - - c.*326C>G p.(=) - - - -
./. - - c.*349G>A p.(=) - - - -
./. - - c.*385_*386insT p.(=) - - - -
./. - - c.*425G>T p.(=) - - - -
./. - - c.*464G>A p.(=) - - - -
./. - - c.*570T>C p.(=) - - - -
./. - - c.*612C>T p.(=) - - - -
./. - - c.*613G>A p.(=) - - - -
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