Transcript #00018678 (NM_006640.4, SEPT9 gene)

Transcript name transcript variant 3
Gene name SEPT9 (septin 9)
Chromosome 17
Transcript - NCBI ID NM_006640.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_006631.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

142 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-38798A>C r.(?) p.(=)
-/. - c.-38798A>C r.(=) p.(=)
?/. - c.-38771del r.(?) p.(=)
-/. - c.-38431T>A r.(?) p.(=)
?/. - c.-32229C>T r.(=) p.(=)
-/. - c.-13307G>A r.(?) p.(=)
-?/. - c.-13205C>T r.(?) p.(=)
?/. - c.-13178C>T r.(?) p.(=)
?/. - c.-13148G>T r.(?) p.(=)
-/. - c.-13111T>C r.(?) p.(=)
-/. - c.-13111T>C r.(?) p.(=)
-/. - c.-12907G>A r.(?) p.(=)
?/. - c.-851C>T r.(=) p.(=)
+/. - c.-134G>C r.(?) p.(=)
-?/. - c.-20_-16dup r.(?) p.(=)
-?/. - c.22+20C>T r.(=) p.(=)
-/. - c.23-28563T>C r.(=) p.(=)
-/. - c.23-28563T>C r.(=) p.(=)
?/. - c.23-28440C>T r.(=) p.(=)
-/. - c.23-26011del r.(=) p.(=)
-/. - c.23-25802C>T r.(=) p.(=)
-/. - c.23-25694G>A r.(=) p.(=)
?/. - c.99A>G r.(=) p.(=)
-?/. - c.147C>T r.(?) p.(Gly49=)
-/. - c.147C>T r.(?) p.(Gly49=)
-?/. - c.162A>G r.(?) p.(=)
?/. - c.169G>T r.(?) p.(Ala57Ser)
-/. - c.214C>T r.(?) p.(Leu72=)
+/. - c.262C>T r.(?) p.(Arg88Trp)
+/. - c.262C>T r.(?) p.(Arg88Trp)
+/. - c.262C>T r.(?) p.(Arg88Trp)
+/. - c.278C>T r.(?) p.(Ser93Phe)
?/. - c.293C>T r.(?) p.(Ser98Phe)
?/. - c.299A>C r.(?) p.(Gln100Pro)
+?/. - c.299_300delinsCC r.(?) p.(Gln100Pro)
+?/. - c.299_300delinsCC r.(?) p.(Gln100Pro)
?/. - c.300G>C r.(?) p.(Gln100His)
-/. - c.380C>T r.(?) p.(Pro127Leu)
?/. - c.406A>G r.(?) p.(Ile136Val)
-?/. - c.460G>A r.(?) p.(Val154Ile)
?/. - c.490G>A r.(?) p.(Asp164Asn)
-?/. - c.546C>T r.(?) p.(Thr182=)
-?/. - c.546C>T r.(?) p.(Thr182=)
?/. - c.546C>T r.(=) p.(=)
-/. - c.633C>T r.(?) p.(Pro211=)
-/. - c.656G>A r.(?) p.(Arg219Gln)
-?/. - c.656G>A r.(?) p.(Arg219Gln)
-/. - c.667+2405G>A r.(=) p.(=)
-/. - c.667+2405G>A r.(=) p.(=)
-/. - c.667+2406C>T r.(=) p.(=)
?/. - c.667+2414C>A r.(=) p.(=)
?/. - c.668-6608G>A r.(=) p.(=)
-?/. - c.668-6590C>T r.(=) p.(=)
-/. - c.668-6464G>A r.(=) p.(=)
-?/. - c.668-6458C>T r.(=) p.(=)
-?/. - c.678G>A r.(?) p.(Ala226=)
-?/. - c.853G>A r.(?) p.(Val285Met)
-?/. - c.853G>A r.(?) p.(Val285Met)
-/. - c.859+64C>T r.(=) p.(=)
-/. - c.859+277T>C r.(=) p.(=)
-?/. - c.860-4C>T r.spl? p.?
-?/. - c.860-4C>T r.spl? p.?
-/. - c.882C>T r.(?) p.(Ser294=)
?/. - c.920G>A r.(?) p.(Arg307Gln)
?/. - c.920G>A r.(?) p.(Arg307Gln)
-/. - c.988+10C>T r.(=) p.(=)
-/. - c.989-321G>A r.(=) p.(=)
-/. - c.989-249T>C r.(=) p.(=)
-/. - c.989-166C>T r.(=) p.(=)
-/. - c.989-119del r.(=) p.(=)
-?/. - c.989-18G>T r.(=) p.(=)
-?/. - c.989-15C>T r.(=) p.(=)
-/. - c.989-4G>A r.spl? p.?
-?/. - c.1009C>T r.(?) p.(Arg337Trp)
?/. - c.1010G>A r.(?) p.(Arg337Gln)
-/. - c.1071-109A>G r.(=) p.(=)
-/. - c.1071-28T>C r.(=) p.(=)
-/. - c.1071-17C>A r.(=) p.(=)
-/. - c.1071-5C>T r.spl? p.?
-?/. - c.1071-5C>T r.spl? p.?
-?/. - c.1071-5C>T r.spl? p.?
?/. - c.1097A>G r.(?) p.(Asn366Ser)
-?/. - c.1107C>T r.(?) p.(Tyr369=)
-?/. - c.1194C>T r.(?) p.(Pro398=)
-/. - c.1208+19G>A r.(=) p.(=)
-/. - c.1208+68A>C r.(=) p.(=)
-/. - c.1208+192del r.(=) p.(=)
-/. - c.1209-143C>T r.(=) p.(=)
?/. - c.1209-57_1209-56insC r.(=) p.(=)
-/. - c.1326+261G>C r.(=) p.(=)
-?/. - c.1344G>A r.(?) p.(Leu448=)
?/. - c.1391C>T r.(?) p.Ser464Leu
?/. - c.1406T>C r.(?) p.(Val469Ala)
?/. - c.1406T>C r.(?) p.(Val469Ala)
-?/. - c.1419C>T r.(?) p.(Phe473=)
?/. - c.1421G>C r.(?) p.(Arg474Pro)
-/. - c.1423-89C>T r.(=) p.(=)
-/. - c.1423-47T>C r.(=) p.(=)
?/. - c.1454A>C r.(?) p.(Asp485Ala)
+?/. - c.1519+2T>A r.spl? p.?
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