Transcript #00000408

Transcript name aarF domain containing kinase 3
Gene name ADCK3 (aarF domain containing kinase 3)
Chromosome 1
Transcript - NCBI ID NM_020247.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_064632.2
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.-137C>A p.(=) - - - -
./. - - c.-113A>G p.(=) - - - -
./. - - c.-75C>T p.(=) - - - -
./. - - c.-10+8T>C p.(=) - - - -
./. - - c.63G>A p.(=) - - - -
./. - - c.117G>A p.(=) - - - -
./. - - c.220G>A p.(Gly74Ser) - - - -
./. - - c.238C>T p.(His80Tyr) - - - -
./. - - c.255T>G p.(His85Gln) - - - -
./. - - c.258A>C p.(=) - - - -
./. - - c.291C>T p.(=) - - - -
./. - - c.358G>A p.(Val120Met) - - - -
./. - - c.427G>A p.(Gly143Arg) - - - -
./. - - c.500_521delinsTTG p.(Gln167Leufs*36) - - - -
./. - - c.521C>A p.(Thr174Lys) - - - -
./. - - c.633_640del p.(Arg213Glnfs*71) - - - -
+/+ - 4/15 c.637C>T p.(Arg213Trp) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.637C>T p.(Arg213Trp) - - - -
./. - - c.687G>A p.(=) - - - -
./. - - c.697G>A p.(Ala233Thr) - - - -
./. - - c.719A>C p.(Glu240Ala) - - - -
./. - - c.798G>A p.(=) - - - -
./. - - c.811C>T p.(Arg271Cys) - - - -
./. - - c.815G>A p.(Gly272Asp) - - - -
+/+ - 11/20 c.815G>A p.(Gly272Asp) probably_damaging(1) missense_variant - deleterious(0)
+/+ - 11/20 c.815G>T p.(Gly272Val) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.815G>T p.(Gly272Val) - - - -
./. - - c.830T>C p.(Leu277Pro) - - - -
./. - - c.895C>T p.(Arg299Trp) - - - -
./. - - c.901C>T p.(Arg301Trp) - - - -
./. - - c.993C>T p.(=) - - - -
+/+ - 13/20 c.993C>T p.(=) - synonymous_variant - -
./. - - c.1000C>T p.(Arg334Trp) - - - -
./. - - c.1006del p.(Phe336Serfs*14) - - - -
./. - - c.1042C>T p.(Arg348*) - - - -
./. - - c.1053C>T p.(=) - - - -
./. - - c.1060G>A p.(Glu354Lys) - - - -
./. - - c.1081-3_1081-2insAGT p.? - - - -
./. - - c.1136T>A p.(Leu379*) - - - -
./. - - c.1163-10C>T p.(=) - - - -
./. - - c.1185C>T p.(=) - - - -
./. - - c.1188C>T p.(=) - - - -
./. - - c.1229G>A p.(Arg410Gln) - - - -
./. - - c.1256+11C>G p.(=) - - - -
./. - - c.1258G>A p.(Asp420Asn) - - - -
./. - - c.1286A>G p.(Tyr429Cys) - - - -
./. - - c.1332_1333del p.(Thr445Argfs*52) - - - -
./. - - c.1396del p.(Glu466Argfs*11) - - - -
./. - - c.1398+2T>C p.? - - - -
./. - - c.1398+12C>A p.(=) - - - -
./. - - c.1399-13G>A p.(=) - - - -
./. - - c.1440C>T p.(=) - - - -
./. - - c.1506+1G>A p.? - - - -
./. - - c.1523T>C p.(Phe508Ser) - - - -
./. - - c.1532C>T p.(Thr511Met) - - - -
./. - - c.1541A>G p.(Tyr514Cys) - - - -
+/+ - 18/20 c.1541A>G p.(Tyr514Cys) probably_damaging(0.978) missense_variant - deleterious(0)
./. - - c.1573-20C>G p.(=) - - - -
./. - - c.1644C>T p.(=) - - - -
./. - - c.1645G>A p.(Gly549Ser) - - - -
+/+ - 19/20 c.1645G>A p.(Gly549Ser) probably_damaging(0.991) missense_variant - deleterious(0)
./. - - c.1651G>A p.(Glu551Lys) - - - -
+/+ - 19/20 c.1651G>A p.(Glu551Lys) probably_damaging(0.996) missense_variant - deleterious(0)
./. - - c.1660-9T>C p.(=) - - - -
./. - - c.1665G>A p.(Met555Ile) - - - -
./. - - c.1679T>C p.(Leu560Ser) - - - -
./. - - c.1711G>A p.(Ala571Thr) - - - -
./. - - c.1713C>A p.(=) - - - -
./. - - c.1716T>C p.(=) - - - -
./. - - c.1741_1742insA p.(Ser582Glufs*148) - - - -
./. - - c.1746_1748del p.(Thr584del) - - - -
?/? - - c.1747_1749del p.(Thr584del) - - - -
?/? - - c.1750_1752del p.(Thr584del) - - - -
./. - - c.1800C>T p.(=) - - - -
./. - - c.1809C>T p.(=) - - - -
?/? - 20/20 c.1811_1812insG p.(Glu605Glyfs*125) - frameshift_variant - -
./. - - c.1811_1812insG p.(Glu605Glyfs*125) - - - -
?/? - - c.1813dup p.(Glu605Glyfs*125) - - - -
./. - 20/20 c.1813_1814insGA p.(Glu605Glyfs*20) - frameshift_variant - -
./. - - c.1838_1839insG p.(Ser616Leufs*114) - - - -
./. - - c.1844G>A p.(Gly615Asp) - - - -
./. - - c.1865_1866insGCT p.(Leu623dup) - - - -
./. - - c.1914C>T p.(=) - - - -
./. - - c.1939C>T p.(Gln647*) - - - -
./. - - c.1942T>G p.(*648Gluext*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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