Transcript #00003279

Transcript name CHK2 checkpoint homolog (S. pombe), transcript variant 3
Gene name CHEK2 (checkpoint kinase 2)
Chromosome 22
Transcript - NCBI ID NM_001005735.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001005735.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-6-43T>C r.(=) p.(=)
?/? c.-6-13C>T r.(=) p.(=)
?/? c.-6G>A r.(=) p.(=)
?/? c.-4C>T r.(=) p.(=)
?/? c.7C>T r.(?) p.(Arg3Trp)
?/? c.14C>T r.(?) p.(Ser5Leu)
?/? c.15G>A r.(=) p.(=)
?/? c.32A>G r.(?) p.(Gln11Arg)
?/? c.79C>G r.(?) p.(Gln27Glu)
?/? c.152del r.(?) p.(Gln51Argfs*10)
?/? c.157T>A r.(?) p.(Ser53Thr)
?/? c.176C>A r.(?) p.(Thr59Lys)
?/? c.190G>A r.(?) p.(Glu64Lys)
?/? c.247del r.(?) p.(Gln83Lysfs*54)
?/? c.252A>G r.(=) p.(=)
?/? c.254C>T r.(?) p.(Pro85Leu)
?/? c.277del r.(?) p.(Trp93Glyfs*44)
?/? c.319+43_319+44insA r.(=) p.(=)
?/? c.449-5T>A r.spl? p.?
?/? c.478A>G r.(?) p.(Arg160Gly)
?/? c.485A>G r.(?) p.(Lys162Arg)
?/? c.518T>A r.(?) p.(Leu173Gln)
?/? c.529G>C r.(?) p.(Asp177His)
?/? c.539G>A r.(?) p.(Arg180Gln)
?/? c.562C>T r.(?) p.(Arg188Trp)
?/? c.572G>T r.(?) p.(Arg191Met)
?/? c.573+19T>C r.(=) p.(=)
?/? c.573+24C>T r.(=) p.(=)
?/? c.573+49T>G r.(=) p.(=)
?/? c.574-50C>G r.(=) p.(=)
?/? c.574-40_574-39del r.(=) p.(=)
?/? c.599T>C r.(?) p.(Ile200Thr)
?/? c.600T>C r.(=) p.(=)
?/? c.612_614del r.(?) p.(Glu204del)
?/? c.628G>A r.(?) p.(Gly210Arg)
?/? c.629G>A r.(?) p.(Gly210Glu)
?/? c.653_654insT r.(?) p.(Gly219Argfs*10)
?/? c.667C>T r.(?) p.(Arg223Cys)
?/? c.670C>T r.(?) p.(Arg224Cys)
?/? c.671G>A r.(?) p.(Arg224His)
?/? c.674C>A r.(?) p.(Pro225His)
?/? c.685A>C r.(?) p.(Asn229His)
?/? c.686A>G r.(?) p.(Asn229Ser)
?/? c.720del r.(?) p.(Val241Phefs*7)
?/? c.721+4A>G r.spl? p.?
?/? c.721+39del r.(=) p.(=)
?/? c.721+39dup r.(=) p.(=)
?/? c.721+50A>T r.(=) p.(=)
?/? c.722-20_722-18del r.(=) p.(=)
?/? c.722-14C>T r.(=) p.(=)
?/? c.722-11_722-7del r.(=) p.(=)
?/? c.729C>G r.(=) p.(=)
?/? c.790A>G r.(?) p.(Ile264Val)
?/? c.792C>G r.(?) p.(Ile264Met)
?/? c.812+46A>G r.(=) p.(=)
?/? c.813-37del r.(=) p.(=)
?/? c.844G>A r.(?) p.(Glu282Lys)
?/? c.855A>G r.(=) p.(=)
?/? c.856T>C r.(?) p.(Cys286Arg)
?/? c.921+24C>T r.(=) p.(=)
?/? c.921+32A>G r.(=) p.(=)
?/? c.921+40G>A r.(=) p.(=)
?/? c.921+42C>G r.(=) p.(=)
?/? c.922-11G>A r.(=) p.(=)
?/? c.975+22A>G r.(=) p.(=)
?/? c.975+35T>C r.(=) p.(=)
?/? c.975+47T>C r.(=) p.(=)
?/? c.976-29C>T r.(=) p.(=)
?/? c.1081C>T r.(?) p.(Arg361Cys)
?/? c.1082G>A r.(?) p.(Arg361His)
?/? c.1091A>C r.(?) p.(Glu364Ala)
?/? c.1137+13C>T r.(=) p.(=)
?/? c.1138-29C>A r.(=) p.(=)
?/? c.1142T>A r.(?) p.(Leu381His)
?/? c.1144C>T r.(?) p.(His382Tyr)
?/? c.1152C>T r.(=) p.(=)
?/? c.1156A>G r.(?) p.(Ile386Val)
?/? c.1224+32C>G r.(=) p.(=)
?/? c.1229del r.(?) p.(Thr410Metfs*15)
?/? c.1244C>T r.(?) p.(Ser415Phe)
?/? c.1270A>G r.(?) p.(Met424Val)
?/? c.1283G>A r.(?) p.(Cys428Tyr)
?/? c.1304C>T r.(?) p.(Ala435Val)
?/? c.1305G>A r.(=) p.(=)
?/? c.1343A>G r.(?) p.(Asn448Ser)
?/? c.1346G>A r.(?) p.(Arg449His)
?/? c.1361G>A r.(?) p.(Trp454*)
?/? c.1388+8A>G r.(=) p.(=)
?/? c.1389-50C>A r.(=) p.(=)
?/? c.1392del r.(?) p.(Ser465Valfs*15)
?/? c.1399T>C r.(?) p.(Tyr467His)
?/? c.1412C>T r.(?) p.(Ser471Phe)
?/? c.1441G>T r.(?) p.(Asp481Tyr)
?/? c.1472T>G r.(?) p.(Ile491Ser)
?/? c.1481T>C r.(?) p.(Val494Ala)
?/? c.1497_1498insA r.(?) p.(Glu500Argfs*33)
?/? c.1536G>A r.(=) p.(=)
?/? c.1550G>A r.(?) p.(Arg517His)
?/? c.1552T>A r.(?) p.(Phe518Ile)
?/? c.1556C>T r.(?) p.(Thr519Met)
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