Transcript #00002803 (NM_016161.2, A4GNT gene)

Transcript name alpha-1,4-N-acetylglucosaminyltransferase
Gene name A4GNT (alpha-1,4-N-acetylglucosaminyltransferase)
Chromosome 3
Transcript - NCBI ID NM_016161.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_057245.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-07 12:22:06 +02:00 (CEST)
Date last edited N/A


Variants

308 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-26-23T>C r.(=) p.(=)
./. c.-23C>T r.(=) p.(=)
./. c.-11G>C r.(=) p.(=)
./. c.-1C>T r.(=) p.(=)
./. c.1A>G r.(?) p.(Met1?)
./. c.4C>T r.(?) p.(Arg2Trp)
./. c.4C>A r.(?) p.(Arg2=)
./. c.5G>A r.(?) p.(Arg2Gln)
./. c.8A>C r.(?) p.(Lys3Thr)
./. c.10G>A r.(?) p.(Glu4Lys)
./. c.20T>G r.(?) p.(Leu7Arg)
./. c.25C>G r.(?) p.(Leu9Val)
./. c.25C>T r.(?) p.(Leu9=)
./. c.42_55del r.(?) p.(Leu15ProfsTer61)
./. c.53G>C r.(?) p.(Gly18Ala)
./. c.60C>T r.(?) p.(Leu20=)
./. c.61T>C r.(?) p.(Tyr21His)
./. c.69C>T r.(?) p.(Phe23=)
./. c.70A>T r.(?) p.(Thr24Ser)
./. c.71C>A r.(?) p.(Thr24Asn)
./. c.75G>C r.(?) p.(Leu25=)
./. c.76A>G r.(?) p.(Lys26Glu)
./. c.80C>G r.(?) p.(Ser27Cys)
./. c.94T>C r.(?) p.(Cys32Arg)
./. c.96T>C r.(?) p.(Cys32=)
./. c.100C>T r.(?) p.(Pro34Ser)
./. c.106T>A r.(?) p.(Phe36Ile)
./. c.108C>T r.(?) p.(Phe36=)
./. c.114C>T r.(?) p.(Ser38=)
./. c.122G>C r.(?) p.(Gly41Ala)
./. c.123G>A r.(?) p.(Gly41=)
./. c.124C>T r.(?) p.(Leu42=)
./. c.135C>G r.(?) p.(Leu45=)
./. c.135C>T r.(?) p.(Leu45=)
./. c.136C>G r.(?) p.(Leu46Val)
./. c.140G>C r.(?) p.(Ser47Thr)
./. c.144C>T r.(?) p.(His48=)
./. c.145A>G r.(?) p.(Arg49Gly)
./. c.146G>T r.(?) p.(Arg49Ile)
./. c.148C>T r.(?) p.(Arg50Cys)
./. c.149G>A r.(?) p.(Arg50His)
./. c.155T>C r.(?) p.(Ile52Thr)
./. c.158T>C r.(?) p.(Val53Ala)
./. c.178A>G r.(?) p.(Arg60Gly)
./. c.179G>A r.(?) p.(Arg60Lys)
./. c.184G>A r.(?) p.(Glu62Lys)
./. c.184G>C r.(?) p.(Glu62Gln)
./. c.189A>T r.(?) p.(Pro63=)
./. c.191C>T r.(?) p.(Pro64Leu)
./. c.191C>A r.(?) p.(Pro64His)
./. c.192C>T r.(?) p.(Pro64=)
./. c.193C>A r.(?) p.(His65Asn)
./. c.193C>T r.(?) p.(His65Tyr)
./. c.194A>G r.(?) p.(His65Arg)
./. c.195T>G r.(?) p.(His65Gln)
./. c.203C>A r.(?) p.(Ser68Tyr)
./. c.205T>G r.(?) p.(Cys69Gly)
./. c.207T>G r.(?) p.(Cys69Trp)
./. c.210C>G r.(?) p.(Ser70=)
./. c.210C>T r.(?) p.(Ser70=)
./. c.211G>A r.(?) p.(Val71Ile)
./. c.213A>T r.(?) p.(Val71=)
./. c.213A>G r.(?) p.(Val71=)
./. c.214G>A r.(?) p.(Glu72Lys)
./. c.215A>G r.(?) p.(Glu72Gly)
./. c.236C>T r.(?) p.(Pro79Leu)
./. c.238G>A r.(?) p.(Glu80Lys)
./. c.247G>C r.(?) p.(Val83Leu)
./. c.249G>A r.(?) p.(Val83=)
./. c.266G>A r.(?) p.(Gly89Asp)
./. c.271A>G r.(?) p.(Thr91Ala)
./. c.272C>T r.(?) p.(Thr91Ile)
./. c.274G>T r.(?) p.(Asp92Tyr)
./. c.274G>A r.(?) p.(Asp92Asn)
./. c.278C>T r.(?) p.(Ser93Phe)
./. c.284C>T r.(?) p.(Pro95Leu)
./. c.284C>A r.(?) p.(Pro95Gln)
./. c.285G>A r.(?) p.(Pro95=)
./. c.291C>A r.(?) p.(Pro97=)
./. c.300C>T r.(?) p.(Ser100=)
./. c.304T>C r.(?) p.(Tyr102His)
./. c.306C>G r.(?) p.(Tyr102Ter)
./. c.310G>C r.(?) p.(Ala104Pro)
./. c.318C>G r.(?) p.(Ser106=)
./. c.318C>T r.(?) p.(Ser106=)
./. c.323T>C r.(?) p.(Leu108Pro)
./. c.332T>C r.(?) p.(Ile111Thr)
./. c.334G>C r.(?) p.(Asp112His)
./. c.334G>A r.(?) p.(Asp112Asn)
./. c.339C>T r.(?) p.(Asn113=)
./. c.340G>A r.(?) p.(Val114Ile)
./. c.340G>C r.(?) p.(Val114Leu)
./. c.344T>A r.(?) p.(Phe115Tyr)
./. c.345C>T r.(?) p.(Phe115=)
./. c.352C>T r.(?) p.(Pro118Ser)
./. c.353C>T r.(?) p.(Pro118Leu)
./. c.368G>C r.(?) p.(Arg123Thr)
./. c.369G>T r.(?) p.(Arg123Ser)
./. c.370C>G r.(?) p.(Leu124Val)
./. c.383C>A r.(?) p.(Thr128Lys)
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