Transcript #00010302

Transcript name MICAL C-terminal like
Gene name MICALCL (MICAL C-terminal like)
Chromosome 11
Transcript - NCBI ID NM_032867.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_116256.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-20C>T r.(=) p.(=)
?/? c.19C>T r.(?) p.(Pro7Ser)
?/? c.122C>T r.(?) p.(Pro41Leu)
?/? c.123G>A r.(=) p.(=)
?/? c.129+1G>A r.spl? p.?
?/? c.129+19C>A r.(=) p.(=)
?/? c.129+43C>G r.(=) p.(=)
?/? c.130-21A>G r.(=) p.(=)
?/? c.161C>T r.(?) p.(Ser54Leu)
?/? c.162G>A r.(=) p.(=)
?/? c.197G>A r.(?) p.(Arg66Gln)
?/? c.203G>A r.(?) p.(Arg68Gln)
?/? c.207C>T r.(=) p.(=)
?/? c.208G>A r.(?) p.(Val70Ile)
?/? c.229G>C r.(?) p.(Glu77Gln)
?/? c.238C>G r.(?) p.(Leu80Val)
?/? c.245T>C r.(?) p.(Leu82Pro)
?/? c.278A>C r.(?) p.(Tyr93Ser)
?/? c.308T>G r.(?) p.(Leu103Arg)
?/? c.341G>T r.(?) p.(Cys114Phe)
?/? c.357C>A r.(=) p.(=)
?/? c.362T>C r.(?) p.(Leu121Pro)
?/? c.366G>A r.(=) p.(=)
?/? c.372C>G r.(?) p.(Ile124Met)
?/? c.402C>G r.(?) p.(Ile134Met)
?/? c.410A>G r.(?) p.(Lys137Arg)
?/? c.429G>C r.(=) p.(=)
?/? c.439T>A r.(?) p.(Ser147Thr)
?/? c.461G>A r.(?) p.(Arg154Gln)
?/? c.532C>T r.(=) p.(=)
?/? c.544G>A r.(?) p.(Val182Ile)
?/? c.632C>T r.(?) p.(Ser211Phe)
?/? c.664C>T r.(?) p.(Arg222Cys)
?/? c.665G>A r.(?) p.(Arg222His)
?/? c.682C>T r.(?) p.(Arg228Cys)
?/? c.683G>A r.(?) p.(Arg228His)
?/? c.738C>T r.(=) p.(=)
?/? c.756C>A r.(=) p.(=)
?/? c.782G>A r.(?) p.(Arg261Gln)
?/? c.786C>T r.(=) p.(=)
?/? c.787G>A r.(?) p.(Val263Met)
?/? c.811C>T r.(?) p.(Arg271Trp)
?/? c.860A>G r.(?) p.(Asn287Ser)
?/? c.870C>T r.(=) p.(=)
?/? c.880G>A r.(?) p.(Ala294Thr)
?/? c.885G>A r.(?) p.(Trp295*)
?/? c.913G>A r.(?) p.(Ala305Thr)
?/? c.929G>A r.(?) p.(Arg310His)
?/? c.937A>G r.(?) p.(Ser313Gly)
?/? c.967G>A r.(?) p.(Gly323Arg)
?/? c.1031G>A r.(?) p.(Arg344His)
?/? c.1032C>T r.(=) p.(=)
?/? c.1051C>T r.(?) p.(Arg351Trp)
?/? c.1052G>A r.(?) p.(Arg351Gln)
?/? c.1067T>A r.(?) p.(Phe356Tyr)
?/? c.1073C>A r.(?) p.(Ala358Glu)
?/? c.1074A>C r.(=) p.(=)
?/? c.1077T>C r.(=) p.(=)
?/? c.1107T>A r.(?) p.(Asp369Glu)
?/? c.1111C>T r.(?) p.(Pro371Ser)
?/? c.1131G>A r.(=) p.(=)
?/? c.1141G>A r.(?) p.(Glu381Lys)
?/? c.1157C>G r.(?) p.(Ala386Gly)
?/? c.1166C>T r.(?) p.(Pro389Leu)
?/? c.1168C>A r.(?) p.(Pro390Thr)
?/? c.1193_1194insA r.(?) p.(Ser399Leufs*10)
?/? c.1226G>A r.(?) p.(Ser409Asn)
?/? c.1233C>T r.(=) p.(=)
?/? c.1267C>G r.(?) p.(Leu423Val)
?/? c.1283A>G r.(?) p.(Lys428Arg)
?/? c.1357C>T r.(?) p.(Arg453Cys)
?/? c.1367_1378del r.(?) p.(Pro467_Pro470del)
?/? c.1369C>G r.(?) p.(Pro457Ala)
?/? c.1370_1378del r.(?) p.(Pro468_Pro470del)
?/? c.1376_1378del r.(?) p.(Pro470del)
?/? c.1376_1378dup r.(?) p.(Pro470dup)
?/? c.1389T>C r.(=) p.(=)
?/? c.1406_1411del r.(?) p.(Pro470_Thr471del)
?/? c.1409_1411del r.(?) p.(Thr471del)
?/? c.1411A>C r.(?) p.(Thr471Pro)
?/? c.1427-31A>C r.(=) p.(=)
?/? c.1427-26_1427-25insT r.(=) p.(=)
?/? c.1427-14T>C r.(=) p.(=)
?/? c.1443C>T r.(=) p.(=)
?/? c.1488C>T r.(=) p.(=)
?/? c.1543-49C>T r.(=) p.(=)
?/? c.1543-28T>A r.(=) p.(=)
?/? c.1543-14A>G r.(=) p.(=)
?/? c.1635+12A>T r.(=) p.(=)
?/? c.1635+54C>T r.(=) p.(=)
?/? c.1636-12C>T r.(=) p.(=)
?/? c.1669C>T r.(?) p.(Arg557Trp)
?/? c.1712C>T r.(?) p.(Ala571Val)
?/? c.1717C>T r.(?) p.(Arg573*)
?/? c.1729+4C>T r.spl? p.?
?/? c.1729+5G>A r.spl? p.?
?/? c.1729+20C>T r.(=) p.(=)
?/? c.1729+55C>T r.(=) p.(=)
?/? c.1730-35C>T r.(=) p.(=)
?/? c.1730-33A>G r.(=) p.(=)
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