Transcript #00016336 (NM_001173466.1, AAAS gene)

Transcript name achalasia, adrenocortical insufficiency, alacrimia, transcript variant 2
Gene name AAAS (aladin WD repeat nucleoporin)
Chromosome 12
Transcript - NCBI ID NM_001173466.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001166937.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 07:58:14 +02:00 (CEST)
Date last edited N/A


Variants

1163 entries on 12 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-51G>A r.(=) p.(=)
./. c.-48G>A r.(=) p.(=)
./. c.-48G>T r.(=) p.(=)
./. c.-48G>C r.(=) p.(=)
./. c.-45C>T r.(=) p.(=)
./. c.-37G>A r.(=) p.(=)
./. c.-35G>A r.(=) p.(=)
./. c.-29C>T r.(=) p.(=)
./. c.-29C>G r.(=) p.(=)
./. c.-20A>G r.(=) p.(=)
./. c.-7C>T r.(=) p.(=)
./. c.-6G>T r.(=) p.(=)
./. c.-4C>G r.(=) p.(=)
./. c.835delCinsT r.(?) p.(Arg279Ter)
./. c.835delCinsG r.(?) p.(Arg279Gly)
./. c.711+17delCinsT r.(=) p.(=)
./. c.673delCinsT r.(?) p.(Arg225Trp)
./. c.664delAinsG r.(?) p.(Ser222Gly)
./. c.*11delGinsA r.(=) p.(=)
./. c.54delAinsG r.(?) p.(Leu18=)
./. c.1399delCinsT r.(?) p.(Arg467Trp)
./. c.969delGinsA r.(?) p.(Leu323=)
./. c.1371delGinsA r.(?) p.(Gln457=)
./. c.1350delGinsA r.(?) p.(Pro450=)
./. c.897+8delGinsA r.(=) p.(=)
./. c.1A>G r.(?) p.(Met1?)
./. c.3G>A r.(?) p.(Met1?)
./. c.4T>G r.(?) p.(Cys2Gly)
./. c.4T>C r.(?) p.(Cys2Arg)
./. c.16T>C r.(?) p.(Leu6=)
./. c.21C>G r.(?) p.(Phe7Leu)
./. c.21C>A r.(?) p.(Phe7Leu)
./. c.25C>T r.(?) p.(Pro9Ser)
./. c.26C>T r.(?) p.(Pro9Leu)
./. c.26C>G r.(?) p.(Pro9Arg)
./. c.30A>G r.(?) p.(Pro10=)
./. c.31C>T r.(?) p.(Pro11Ser)
./. c.32C>A r.(?) p.(Pro11Gln)
./. c.35C>T r.(?) p.(Pro12Leu)
./. c.35C>G r.(?) p.(Pro12Arg)
./. c.36T>G r.(?) p.(Pro12=)
./. c.38G>C r.(?) p.(Arg13Pro)
./. c.43C>A r.(?) p.(Gln15Lys)
./. c.43C>T r.(?) p.(Gln15Ter)
./. c.51C>T r.(?) p.(Thr17=)
./. c.51C>A r.(?) p.(Thr17=)
./. c.52C>T r.(?) p.(Leu18=)
./. c.52_53del r.(?) p.(Leu18IlefsTer2)
./. c.56A>G r.(?) p.(Tyr19Cys)
./. c.57_58del r.(?) p.(Tyr19Ter)
./. c.58G>C r.(?) p.(Glu20Gln)
./. c.61_62insTGGTG r.(?) p.(His21LeufsTer8)
./. c.63C>G r.(?) p.(His21Gln)
./. c.63C>T r.(?) p.(His21=)
./. c.65A>G r.(?) p.(Asn22Ser)
./. c.66T>A r.(?) p.(Asn22Lys)
./. c.69C>T r.(?) p.(Asn23=)
./. c.71A>G r.(?) p.(Glu24Gly)
./. c.75G>A r.(?) p.(Leu25=)
./. c.76G>T r.(?) p.(Val26Leu)
./. c.78G>A r.(?) p.(Val26=)
./. c.80C>T r.(?) p.(Thr27Met)
./. c.86G>A r.(?) p.(Ser29Asn)
./. c.90C>T r.(?) p.(Ser30=)
./. c.92A>G r.(?) p.(Tyr31Cys)
./. c.96G>C r.(?) p.(Glu32Asp)
./. c.102G>A r.(?) p.(Pro34=)
./. c.103C>G r.(?) p.(Pro35Ala)
./. c.106C>T r.(?) p.(Pro36Ser)
./. c.107C>T r.(?) p.(Pro36Leu)
./. c.108dupC r.(?) p.(Asp37ArgfsTer50)
./. c.109G>A r.(?) p.(Asp37Asn)
./. c.109G>C r.(?) p.(Asp37His)
./. c.117G>A r.(?) p.(Arg39=)
./. c.120C>T r.(?) p.(Gly40=)
./. c.121C>T r.(?) p.(Gln41Ter)
./. c.123+7A>T r.(=) p.(=)
./. c.123+9_123+27del r.(=) p.(=)
./. c.123+11C>G r.(=) p.(=)
./. c.123+12G>A r.(=) p.(=)
./. c.123+14G>A r.(=) p.(=)
./. c.123+15G>A r.(=) p.(=)
./. c.123+15G>C r.(=) p.(=)
./. c.123+30_123+31del r.(=) p.(=)
./. c.123+34C>T r.(=) p.(=)
./. c.123+35A>G r.(=) p.(=)
./. c.123+35A>C r.(=) p.(=)
./. c.123+41G>A r.(=) p.(=)
./. c.123+50G>A r.(=) p.(=)
./. c.124-48T>A r.(=) p.(=)
./. c.124-47T>A r.(=) p.(=)
./. c.124-47T>C r.(=) p.(=)
./. c.124-43A>G r.(=) p.(=)
./. c.124-39G>T r.(=) p.(=)
./. c.124-39G>A r.(=) p.(=)
./. c.124-37C>T r.(=) p.(=)
./. c.124-33A>C r.(=) p.(=)
./. c.124-31C>T r.(=) p.(=)
./. c.124-28C>A r.(=) p.(=)
./. c.124-28C>T r.(=) p.(=)
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