Transcript #00011887 (NM_138932.2, A1CF gene)

Transcript name transcript variant 2
Gene name A1CF (APOBEC1 complementation factor)
Chromosome 10
Transcript - NCBI ID NM_138932.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_620310.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 00:34:57 +02:00 (CEST)
Date last edited N/A


Variants

700 entries on 7 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-45-4T>C r.(=) p.(=)
./. c.-45-3C>T r.(=) p.(=)
./. c.-43A>G r.(=) p.(=)
./. c.-31T>C r.(=) p.(=)
./. c.-23T>C r.(=) p.(=)
./. c.-13A>G r.(=) p.(=)
./. c.-12_-11insG r.(=) p.(=)
./. c.-8C>A r.(=) p.(=)
./. c.-3T>A r.(=) p.(=)
./. c.-2C>T r.(=) p.(=)
./. c.770-22delCinsT r.(=) p.(=)
./. c.1484+33delAinsC r.(=) p.(=)
./. c.*45delAinsT r.(=) p.(=)
./. c.*42delAinsG r.(=) p.(=)
./. c.*27delGinsA r.(=) p.(=)
./. c.*27delGinsT r.(=) p.(=)
./. c.1141+42delTinsC r.(=) p.(=)
./. c.235-8delAinsG r.(=) p.(=)
./. c.867+50delTinsG r.(=) p.(=)
./. c.151delCinsA r.(?) p.(Pro51Thr)
./. c.151delCinsT r.(?) p.(Pro51Ser)
./. c.1delA r.(?) p.(Met1?)
./. c.1A>G r.(?) p.(Met1?)
./. c.3G>A r.(?) p.(Met1?)
./. c.7T>C r.(?) p.(Ser3Pro)
./. c.11A>G r.(?) p.(Asn4Ser)
./. c.13C>T r.(?) p.(His5Tyr)
./. c.14A>G r.(?) p.(His5Arg)
./. c.18A>G r.(?) p.(Lys6=)
./. c.21C>T r.(?) p.(Ser7=)
./. c.22G>A r.(?) p.(Gly8Arg)
./. c.23G>A r.(?) p.(Gly8Glu)
./. c.24G>A r.(?) p.(Gly8=)
./. c.28G>A r.(?) p.(Gly10Arg)
./. c.30A>C r.(?) p.(Gly10=)
./. c.32T>C r.(?) p.(Leu11Ser)
./. c.36C>T r.(?) p.(Ser12=)
./. c.37G>T r.(?) p.(Gly13Cys)
./. c.37G>A r.(?) p.(Gly13Ser)
./. c.38G>T r.(?) p.(Gly13Val)
./. c.39C>T r.(?) p.(Gly13=)
./. c.51A>C r.(?) p.(Glu17Asp)
./. c.60C>T r.(?) p.(Leu20=)
./. c.63C>T r.(?) p.(Arg21=)
./. c.64G>T r.(?) p.(Ala22Ser)
./. c.65C>A r.(?) p.(Ala22Glu)
./. c.66A>T r.(?) p.(Ala22=)
./. c.66A>C r.(?) p.(Ala22=)
./. c.69G>C r.(?) p.(Leu23=)
./. c.70G>A r.(?) p.(Val24Ile)
./. c.76C>A r.(?) p.(Arg26Ser)
./. c.77G>A r.(?) p.(Arg26His)
./. c.77G>C r.(?) p.(Arg26Pro)
./. c.81A>G r.(?) p.(Thr27=)
./. c.86A>G r.(?) p.(Tyr29Cys)
./. c.93G>C r.(?) p.(Leu31Phe)
./. c.99+8C>T r.(=) p.(=)
./. c.99+12T>C r.(=) p.(=)
./. c.99+17T>A r.(=) p.(=)
./. c.99+19T>C r.(=) p.(=)
./. c.99+20G>C r.(=) p.(=)
./. c.99+20G>T r.(=) p.(=)
./. c.99+22T>C r.(=) p.(=)
./. c.99+27C>T r.(=) p.(=)
./. c.99+28T>C r.(=) p.(=)
./. c.99+31C>T r.(=) p.(=)
./. c.99+34C>T r.(=) p.(=)
./. c.99+35T>C r.(=) p.(=)
./. c.99+35T>A r.(=) p.(=)
./. c.99+47G>A r.(=) p.(=)
./. c.100-47delG r.(=) p.(=)
./. c.100-28C>T r.(=) p.(=)
./. c.100-26C>T r.(=) p.(=)
./. c.100-25C>T r.(=) p.(=)
./. c.100-23T>C r.(=) p.(=)
./. c.108A>G r.(?) p.(Gly36=)
./. c.129T>A r.(?) p.(Pro43=)
./. c.133C>T r.(?) p.(Pro45Ser)
./. c.142G>A r.(?) p.(Asp48Asn)
./. c.148dupG r.(?) p.(Ala50GlyfsTer4)
./. c.150delA r.(?) p.(Pro52LeufsTer34)
./. c.150A>G r.(?) p.(Ala50=)
./. c.152C>T r.(?) p.(Pro51Leu)
./. c.154C>G r.(?) p.(Pro52Ala)
./. c.155dupC r.(?) p.(Glu53Ter)
./. c.161G>A r.(?) p.(Arg54Lys)
./. c.167G>C r.(?) p.(Cys56Ser)
./. c.168T>G r.(?) p.(Cys56Trp)
./. c.170A>C r.(?) p.(Glu57Ala)
./. c.182G>C r.(?) p.(Gly61Ala)
./. c.193C>T r.(?) p.(Arg65Ter)
./. c.194G>A r.(?) p.(Arg65Gln)
./. c.198C>A r.(?) p.(Asp66Glu)
./. c.199delC r.(?) p.(Leu67PhefsTer19)
./. c.199C>T r.(?) p.(Leu67Phe)
./. c.207G>A r.(?) p.(Glu69=)
./. c.208G>A r.(?) p.(Asp70Asn)
./. c.213G>A r.(?) p.(Glu71=)
./. c.214C>T r.(?) p.(Leu72Phe)
./. c.217A>G r.(?) p.(Ile73Val)
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