Transcript #00022673 (NM_012138.3, AATF gene)

Transcript name apoptosis antagonizing transcription factor
Gene name AATF (apoptosis antagonizing transcription factor)
Chromosome 17
Transcript - NCBI ID NM_012138.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_036270.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 21:27:44 +02:00 (CEST)
Date last edited N/A


Variants

719 entries on 8 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-50G>C r.(=) p.(=)
./. c.-41_-33del r.(=) p.(=)
./. c.-39T>A r.(=) p.(=)
./. c.-33G>A r.(=) p.(=)
./. c.-31G>A r.(=) p.(=)
./. c.-18G>C r.(=) p.(=)
./. c.-18G>T r.(=) p.(=)
./. c.-15C>G r.(=) p.(=)
./. c.-15C>T r.(=) p.(=)
./. c.-11A>T r.(=) p.(=)
./. c.1420delCinsT r.(?) p.(Arg474Trp)
./. c.178delGinsA r.(?) p.(Ala60Thr)
./. c.948-9delCinsT r.(=) p.(=)
./. c.283+24delAinsT r.(=) p.(=)
./. c.1547+34delAinsG r.(=) p.(=)
./. c.1076delTinsG r.(?) p.(Phe359Cys)
./. c.1206delCinsG r.(?) p.(Asp402Glu)
./. c.1206delCinsT r.(?) p.(AspLys402=)
./. c.8G>C r.(?) p.(Gly3Ala)
./. c.9G>C r.(?) p.(Gly3=)
./. c.25C>G r.(?) p.(Leu9Val)
./. c.31C>T r.(?) p.(Leu11=)
./. c.44T>G r.(?) p.(Leu15Trp)
./. c.52C>G r.(?) p.(Arg18Gly)
./. c.72_73insGAAGCGGACCCC r.(?) p.(Ala26_Glu29dup)
./. c.75A>G r.(?) p.(Glu25=)
./. c.81C>T r.(?) p.(Asp27=)
./. c.87G>A r.(?) p.(Glu29=)
./. c.88G>A r.(?) p.(Glu30Lys)
./. c.91+14G>C r.(=) p.(=)
./. c.91+17G>A r.(=) p.(=)
./. c.91+17_91+18insT r.(=) p.(=)
./. c.91+34C>G r.(=) p.(=)
./. c.91+44G>A r.(=) p.(=)
./. c.91+46C>G r.(=) p.(=)
./. c.92-47T>G r.(=) p.(=)
./. c.92-43G>A r.(=) p.(=)
./. c.92-41dupT r.(=) p.(=)
./. c.92-38C>G r.(=) p.(=)
./. c.92-29T>C r.(=) p.(=)
./. c.92-26G>A r.(=) p.(=)
./. c.92-16C>T r.(=) p.(=)
./. c.92-11T>G r.(=) p.(=)
./. c.92-10C>T r.(=) p.(=)
./. c.92-6C>T r.(=) p.(=)
./. c.92-3C>A r.spl? p.?
./. c.93C>G r.(?) p.(Ala31=)
./. c.97G>A r.(?) p.(Ala33Thr)
./. c.102C>T r.(?) p.(Ala34=)
./. c.103A>G r.(?) p.(Arg35Gly)
./. c.108G>A r.(?) p.(Val36=)
./. c.109A>T r.(?) p.(Ile37Phe)
./. c.116G>A r.(?) p.(Arg39Lys)
./. c.117G>A r.(?) p.(Arg39=)
./. c.119T>C r.(?) p.(Phe40Ser)
./. c.126A>G r.(?) p.(Glu42=)
./. c.128G>A r.(?) p.(Gly43Glu)
./. c.129G>A r.(?) p.(Gly43=)
./. c.130G>A r.(?) p.(Glu44Lys)
./. c.133G>C r.(?) p.(Asp45His)
./. c.142G>A r.(?) p.(Gly48Ser)
./. c.143G>T r.(?) p.(Gly48Val)
./. c.150C>G r.(?) p.(Phe50Leu)
./. c.156_157insGT r.(?) p.(Gly54TrpfsTer157)
./. c.168T>C r.(?) p.(Ile56=)
./. c.169A>G r.(?) p.(Arg57Gly)
./. c.170G>C r.(?) p.(Arg57Thr)
./. c.175C>G r.(?) p.(Leu59Val)
./. c.177G>A r.(?) p.(Leu59=)
./. c.179delC r.(?) p.(Ala60AspfsTer150)
./. c.179C>T r.(?) p.(Ala60Val)
./. c.181T>A r.(?) p.(Ser61Thr)
./. c.182C>T r.(?) p.(Ser61Leu)
./. c.186C>T r.(?) p.(Ala62=)
./. c.190C>T r.(?) p.(Leu64Phe)
./. c.194T>G r.(?) p.(Leu65Trp)
./. c.199A>G r.(?) p.(Thr67Ala)
./. c.200C>T r.(?) p.(Thr67Met)
./. c.201G>C r.(?) p.(Thr67=)
./. c.201G>A r.(?) p.(Thr67=)
./. c.204C>T r.(?) p.(Asp68=)
./. c.206A>G r.(?) p.(Lys69Arg)
./. c.208A>C r.(?) p.(Arg70=)
./. c.215G>C r.(?) p.(Cys72Ser)
./. c.225C>T r.(?) p.(Thr75=)
./. c.229T>G r.(?) p.(Ser77Ala)
./. c.232A>G r.(?) p.(Arg78Gly)
./. c.237A>G r.(?) p.(Lys79=)
./. c.243G>A r.(?) p.(Trp81Ter)
./. c.246T>C r.(?) p.(Asn82=)
./. c.247G>C r.(?) p.(Glu83Gln)
./. c.250G>A r.(?) p.(Asp84Asn)
./. c.253C>T r.(?) p.(His85Tyr)
./. c.254A>G r.(?) p.(His85Arg)
./. c.255T>C r.(?) p.(His85=)
./. c.256dupT r.(?) p.(Trp86LeufsTer10)
./. c.261G>A r.(?) p.(Glu87=)
./. c.266C>T r.(?) p.(Thr89Ile)
./. c.271C>T r.(?) p.(Pro91Ser)
./. c.275G>A r.(?) p.(Gly92Glu)
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