Transcript #00024647 (NM_001166579.1, AANAT gene)

Transcript name transcript variant 1
Gene name AANAT (aralkylamine N-acetyltransferase)
Chromosome 17
Transcript - NCBI ID NM_001166579.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001160051.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-09 01:10:20 +02:00 (CEST)
Date last edited N/A


Variants

887 entries on 9 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-1682G>C r.(=) p.(=)
./. c.-1646_-1644del r.(=) p.(=)
./. c.-1643_-1642insAA r.(=) p.(=)
./. c.-1591C>T r.(=) p.(=)
./. c.-1576G>C r.(=) p.(=)
./. c.-1561G>C r.(=) p.(=)
./. c.-1522G>A r.(=) p.(=)
./. c.-1450C>G r.(=) p.(=)
./. c.-1441G>C r.(=) p.(=)
./. c.-1408G>A r.(=) p.(=)
./. c.-1398A>T r.(=) p.(=)
./. c.-1378G>C r.(=) p.(=)
./. c.-1366G>A r.(=) p.(=)
./. c.-1365G>A r.(=) p.(=)
./. c.-1362T>G r.(=) p.(=)
./. c.-1340A>C r.(=) p.(=)
./. c.-1310G>A r.(=) p.(=)
./. c.-1291G>A r.(=) p.(=)
./. c.-39delC r.(=) p.(=)
./. c.-39C>T r.(=) p.(=)
./. c.-38G>A r.(=) p.(=)
./. c.-29C>T r.(=) p.(=)
./. c.-20delA r.(=) p.(=)
./. c.-20A>T r.(=) p.(=)
./. c.-18T>G r.(=) p.(=)
./. c.-7G>A r.(=) p.(=)
./. c.-5G>A r.(=) p.(=)
./. c.-4dupT r.(=) p.(=)
./. c.489delAinsG r.(?) p.(Ile163Met)
./. c.84delTinsC r.(?) p.(LeuArg28=)
./. c.84delTinsA r.(?) p.(LeuArg28=)
./. c.221delGinsA r.(?) p.(Arg74His)
./. c.221delGinsC r.(?) p.(Arg74Pro)
./. c.3G>T r.(?) p.(Met1?)
./. c.3G>A r.(?) p.(Met1?)
./. c.23G>C r.(?) p.(Gly8Ala)
./. c.23G>A r.(?) p.(Gly8Glu)
./. c.29A>C r.(?) p.(Lys10Thr)
./. c.50G>A r.(?) p.(Trp17Ter)
./. c.60+3G>T r.spl? p.?
./. c.60+7A>T r.(=) p.(=)
./. c.60+9G>A r.(=) p.(=)
./. c.60+18A>G r.(=) p.(=)
./. c.60+24T>C r.(=) p.(=)
./. c.60+38C>T r.(=) p.(=)
./. c.60+40_60+43del r.(=) p.(=)
./. c.60+45C>T r.(=) p.(=)
./. c.61-49C>T r.(=) p.(=)
./. c.61-37G>A r.(=) p.(=)
./. c.61-33A>T r.(=) p.(=)
./. c.61-25C>T r.(=) p.(=)
./. c.61-19C>T r.(=) p.(=)
./. c.61-17T>C r.(=) p.(=)
./. c.61-6C>A r.(=) p.(=)
./. c.64C>G r.(?) p.(Leu22Val)
./. c.70G>A r.(?) p.(Gly24Ser)
./. c.77C>G r.(?) p.(Pro26Arg)
./. c.85_87del r.(?) p.(Arg30del)
./. c.94C>T r.(?) p.(Leu32Phe)
./. c.96T>G r.(?) p.(Leu32=)
./. c.103C>G r.(?) p.(Leu35Val)
./. c.109C>A r.(?) p.(Arg37Ser)
./. c.109C>T r.(?) p.(Arg37Cys)
./. c.110G>A r.(?) p.(Arg37His)
./. c.113C>T r.(?) p.(Pro38Leu)
./. c.116A>G r.(?) p.(Lys39Arg)
./. c.117G>C r.(?) p.(Lys39Asn)
./. c.118G>A r.(?) p.(Glu40Lys)
./. c.134G>C r.(?) p.(Arg45Thr)
./. c.143C>T r.(?) p.(Thr48Met)
./. c.143C>A r.(?) p.(Thr48Lys)
./. c.144G>A r.(?) p.(Thr48=)
./. c.145C>T r.(?) p.(Gln49Ter)
./. c.150C>G r.(?) p.(Ser50Arg)
./. c.151A>C r.(?) p.(Thr51Pro)
./. c.156C>T r.(?) p.(His52=)
./. c.157C>T r.(?) p.(Pro53Ser)
./. c.170A>G r.(?) p.(Glu57Gly)
./. c.172G>T r.(?) p.(Ala58Ser)
./. c.178C>T r.(?) p.(Arg60Cys)
./. c.179G>A r.(?) p.(Arg60His)
./. c.187C>G r.(?) p.(Pro63Ala)
./. c.191G>A r.(?) p.(Gly64Glu)
./. c.195C>T r.(?) p.(Ile65=)
./. c.195C>A r.(?) p.(Ile65=)
./. c.198C>T r.(?) p.(Pro66=)
./. c.199G>A r.(?) p.(Glu67Lys)
./. c.204C>G r.(?) p.(Ser68=)
./. c.206C>T r.(?) p.(Pro69Leu)
./. c.210C>A r.(?) p.(Ser70Arg)
./. c.211T>A r.(?) p.(Cys71Ser)
./. c.217C>T r.(?) p.(Arg73Trp)
./. c.218G>A r.(?) p.(Arg73Gln)
./. c.220C>T r.(?) p.(Arg74Cys)
./. c.223delC r.(?) p.(His75ThrfsTer45)
./. c.225C>A r.(?) p.(His75Gln)
./. c.225C>T r.(?) p.(His75=)
./. c.227C>T r.(?) p.(Thr76Ile)
./. c.229C>A r.(?) p.(Leu77Ile)
./. c.231C>T r.(?) p.(Leu77=)
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