Transcript #00010257 (NM_002405.3, MFNG gene)

Transcript name transcript variant 1
Gene name MFNG (MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase)
Chromosome 22
Transcript - NCBI ID NM_002405.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002396.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-20T>C r.(=) p.(=)
?/? c.-12C>G r.(=) p.(=)
?/? c.-1A>G r.(=) p.(=)
?/? c.19C>G r.(?) p.(Arg7Gly)
?/? c.45C>T r.(=) p.(=)
?/? c.56T>C r.(?) p.(Met19Thr)
?/? c.67T>G r.(?) p.(Cys23Gly)
?/? c.88C>G r.(?) p.(Leu30Val)
?/? c.101G>A r.(?) p.(Arg34Gln)
?/? c.131C>T r.(?) p.(Pro44Leu)
?/? c.138G>A r.(=) p.(=)
?/? c.159A>C r.(=) p.(=)
?/? c.185C>A r.(?) p.(Thr62Lys)
?/? c.203G>A r.(?) p.(Arg68His)
?/? c.220C>T r.(=) p.(=)
?/? c.249G>A r.(=) p.(=)
?/? c.255G>A r.(=) p.(=)
?/? c.255+5C>T r.spl? p.?
?/? c.255+19T>C r.(=) p.(=)
?/? c.256-55G>A r.(=) p.(=)
?/? c.256-35C>T r.(=) p.(=)
?/? c.256-34G>A r.(=) p.(=)
?/? c.261T>G r.(?) p.(Phe87Leu)
?/? c.304+12C>T r.(=) p.(=)
?/? c.304+13G>A r.(=) p.(=)
?/? c.304+38G>C r.(=) p.(=)
?/? c.304+61C>T r.(=) p.(=)
?/? c.305-40_305-39insG r.(=) p.(=)
?/? c.334G>A r.(?) p.(Ala112Thr)
?/? c.335C>T r.(?) p.(Ala112Val)
?/? c.384C>A r.(?) p.(Asp128Glu)
?/? c.407+2C>T r.spl? p.?
?/? c.407+4A>G r.spl? p.?
?/? c.407+10C>T r.(=) p.(=)
?/? c.407+21G>C r.(=) p.(=)
?/? c.407+39G>A r.(=) p.(=)
?/? c.407+40G>T r.(=) p.(=)
?/? c.408-35C>A r.(=) p.(=)
?/? c.408-17C>G r.(=) p.(=)
?/? c.408-16C>T r.(=) p.(=)
?/? c.408-2A>T r.spl? p.?
?/? c.426C>T r.(=) p.(=)
?/? c.444C>T r.(=) p.(=)
?/? c.446C>A r.(?) p.(Pro149Gln)
?/? c.452C>T r.(?) p.(Ala151Val)
?/? c.480G>A r.(=) p.(=)
?/? c.493G>A r.(?) p.(Val165Ile)
?/? c.498T>C r.(=) p.(=)
?/? c.503G>C r.(?) p.(Gly168Ala)
?/? c.520C>T r.(?) p.(Arg174Trp)
?/? c.556C>T r.(?) p.(Arg186Cys)
?/? c.561+31G>T r.(=) p.(=)
?/? c.561+36G>A r.(=) p.(=)
?/? c.562-15_562-14insC r.(=) p.(=)
?/? c.562-3C>T r.spl? p.?
?/? c.569_577del r.(?) p.(Val190_Trp193delinsGly)
?/? c.578G>A r.(?) p.(Trp193*)
?/? c.611A>G r.(?) p.(Asn204Ser)
?/? c.639G>A r.(=) p.(=)
?/? c.647+31G>T r.(=) p.(=)
?/? c.647+42G>T r.(=) p.(=)
?/? c.648-38G>A r.(=) p.(=)
?/? c.648-26G>A r.(=) p.(=)
?/? c.682C>T r.(?) p.(Arg228Trp)
?/? c.716T>C r.(?) p.(Ile239Thr)
?/? c.731G>A r.(?) p.(Gly244Asp)
?/? c.732C>T r.(=) p.(=)
?/? c.733G>A r.(?) p.(Gly245Ser)
?/? c.813+2del r.spl? p.?
?/? c.814-23C>T r.(=) p.(=)
?/? c.814-20T>G r.(=) p.(=)
?/? c.828C>T r.(=) p.(=)
?/? c.829G>A r.(?) p.(Gly277Ser)
?/? c.854T>A r.(?) p.(Val285Asp)
?/? c.881C>T r.(?) p.(Pro294Leu)
?/? c.882G>A r.(=) p.(=)
?/? c.899+28G>A r.(=) p.(=)
?/? c.899+32G>A r.(=) p.(=)
?/? c.899+45A>C r.(=) p.(=)
?/? c.900-47G>T r.(=) p.(=)
?/? c.900-34G>A r.(=) p.(=)
?/? c.900-8C>T r.(=) p.(=)
?/? c.904C>T r.(?) p.(Arg302Cys)
?/? c.905G>A r.(?) p.(Arg302His)
?/? c.916T>C r.(?) p.(Cys306Arg)
?/? c.942G>A r.(?) p.(Trp314*)
?/? c.961C>T r.(?) p.(Arg321*)
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