Transcript #00013760 (NM_006302.2, MOGS gene)

Transcript name transcript variant 1
Gene name MOGS (mannosyl-oligosaccharide glucosidase)
Chromosome 2
Transcript - NCBI ID NM_006302.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006293.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.12C>G r.(?) p.(Gly4=)
-?/. - c.12C>G r.(?) p.(Gly4=)
-?/. - c.65C>A r.(?) p.(Ala22Glu)
+/. - c.65C>A r.(?) p.(Ala22Glu)
+/. - c.65C>A r.(?) p.(Ala22Glu)
+/. - c.65C>A r.[352_353ins352+1_353-1,=] p.[Leu119fs,=]
-?/. - c.184G>A r.(?) p.(Val62Met)
+/. - c.224A>C r.(?) p.(His75Pro)
+/. - c.329G>A r.(?) p.(Arg110His)
+/. - c.329G>A r.(?) p.(Arg110His)
?/. - c.329G>A r.329g>a p.Arg110His
+/. - c.370C>T r.(?) p.(Gln124Ter)
+/. - c.370C>T r.(?) p.(Gln124*)
?/. - c.407C>T r.(?) p.(Thr136Met)
?/. - c.418G>A r.(?) p.(Gly140Arg)
?/. - c.436T>G r.(?) p.(Tyr146Asp)
+/. - c.480_481del r.(?) p.(Ile161ProfsTer10)
-?/. - c.525G>A r.(?) p.(Arg175=)
+?/. - c.544G>A r.(?) p.(Gly182Arg)
+?/. - c.544G>A r.(?) p.(Gly182Arg)
-?/. - c.870_871insCCTG r.(?) p.(Gly291ProfsTer6)
+/. - c.882del r.(?) p.(Glu295AsnfsTer10)
-?/. - c.894C>T r.(?) p.(Leu298=)
-?/. - c.1000T>G r.(?) p.(Phe334Val)
-?/. - c.1109A>G r.(?) p.(Glu370Gly)
-?/. - c.1197T>C r.(?) p.(Leu399=)
+/. - c.1212_1239dup r.(?) p.(Asp414LeufsTer17)
+/. - c.1212_1239dup r.(?) p.(Asp414LeufsTer17)
+/. - c.1212_1239dup r.(?) p.(Asp414LeufsTer17)
-/. - c.1245C>G r.(?) p.(Ile415Met)
?/. - c.1248_1249insT r.(?) p.(Val417Cysfs*5)
?/. - c.1252del r.(?) p.(Glu418Lysfs*61)
+/. - c.1286_1287del r.(?) p.(Phe429SerfsTer23)
+/. - c.1348T>G r.(?) p.(Trp450Gly)
+/. - c.1457G>A r.(?) p.(Arg486Thr)
+/. - c.1461G>C r.(?) p.(Glu487Asp)
+/. - c.1461G>C r.(?) p.(Glu487Asp)
?/. - c.1472G>T r.(?) p.(Gly491Val)
+/. - c.1483C>T r.(?) p.(Arg495Ter)
+/. - c.1483C>T r.(?) p.(Arg495Ter)
+/. - c.1514_1516del r.(?) p.(Gln505del)
+/. - c.1514_1516del r.(?) p.(Gln505del)
+/. - c.1514_1516del r.(?) p.(Gln505del)
+/. - c.1537C>T r.(?) p.(Pro513Ser)
-?/. - c.1581C>A r.(?) p.(Asp527Glu)
-?/. - c.1581C>A r.(?) p.(Asp527Glu)
+/. - c.1603C>T r.(?) p.(Arg535Ter)
+/. - c.1603C>T r.(?) p.(Arg535Ter)
+/. - c.1603C>T r.(?) p.(Arg535Ter)
+/. - c.1619G>A r.(?) p.(Arg540His)
+/. - c.1619G>A r.(?) p.(Arg540His)
+/. - c.1681C>T r.(?) p.(Arg561Cys)
+/. - c.1694G>A r.(?) p.(Arg565Gln)
?/. - c.1698C>A r.(?) p.(Asp566Glu)
+?/. - c.1698C>A r.(?) p.(Asp566Glu)
+?/. - c.1698C>A r.(?) p.(Asp566Glu)
+/. - c.1766C>T r.(?) p.(Ser589Leu)
+/. - c.1787G>A r.(?) p.(Arg596Gln)
+/. - c.1801C>T r.(?) p.(Arg601Ter)
-?/. - c.1944G>A r.(?) p.(Glu648=)
+/. - c.1954T>C r.(?) p.(Phe652Leu)
-?/. - c.2055T>C r.(?) p.(Tyr685=)
?/. - c.2062G>A r.(?) p.(Ala688Thr)
+/. - c.2090T>C r.(?) p.(Leu697Ser)
+/. - c.2098C>T r.(?) p.(Arg700Ter)
+/. - c.2126T>C r.(?) p.(Leu709Pro)
+/. - c.2255G>A r.(?) p.(Gly752Asp)
-?/. - c.2372T>C r.(?) p.(Val791Ala)
?/. - c.2389C>T r.(?) p.(Arg797Cys)
+/. - c.2405C>T r.(?) p.(Thr802Ile)
+/. - c.2471G>A r.(?) p.(Gly824Asp)
?/. - c.*1569C>T r.(=) p.(=)
?/. - c.*1626C>G r.(=) p.(=)
-?/. - c.*3731G>T r.(=) p.(=)
?/. - c.*3911G>A r.(=) p.(=)
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