Transcript #00025713 (NM_001160372.1, TRAPPC9 gene)

Transcript name transcript variant 2
Gene name TRAPPC9 (trafficking protein particle complex 9)
Chromosome 8
Transcript - NCBI ID NM_001160372.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001153844.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2022-06-27 15:07:22 +02:00 (CEST)
Date last edited N/A


Variants

82 entries on 1 page. Showing entries 1 - 82.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-750A>G r.(?) p.(=)
-?/. - c.-643G>A r.(=) p.(=)
+/. - c.-10-1G>A r.spl? p.?
?/. - c.44C>T r.(?) p.(Thr15Met)
?/. - c.64C>A r.(?) p.(Pro22Thr)
?/. - c.136G>A r.(?) p.(Val46Met)
-?/. - c.140G>A r.(?) p.(Arg47Gln)
-/. - c.207T>C r.(?) p.(Gly69=)
-/. - c.207T>C r.(?) p.(Gly69=)
?/. - c.243C>G r.(?) p.(Ile81Met)
?/. - c.263C>T r.(?) p.(Ser88Leu)
?/. - c.284C>T r.(?) p.(Thr95Ile)
-/. - c.288T>C r.(?) p.(Phe96=)
-/. - c.288T>C r.(?) p.(Phe96=)
+/. - c.331_334del r.(?) p.(Tyr111ThrfsTer77)
-/. - c.357G>A r.(?) p.(Gly119=)
-/. - c.357G>A r.(?) p.(Gly119=)
+/. - c.367G>T r.(?) p.(Glu123*)
-?/. - c.394G>A r.(?) p.(Val132Met)
-/. - c.399T>C r.(?) p.(Ala133=)
-/. - c.399T>C r.(?) p.(Ala133=)
-/. - c.456C>T r.(?) p.(Ile152=)
+?/. 2 c.533T>C r.(?) p.(Leu178Pro)
+?/. - c.533T>C r.(?) p.(Leu178Pro)
-/. - c.555G>A r.(?) p.(Lys185=)
-/. - c.555G>A r.(?) p.(Lys185=)
?/. - c.613A>G r.(?) p.(Met205Val)
+?/. 3 c.623A>C r.(?) p.(His208Pro)
-/. - c.731-31_731-11del r.(=) p.(=)
?/. - c.805C>T r.(?) p.(Arg269Trp)
+/. - c.853C>T r.(?) p.(Arg285Trp)
?/. - c.853C>T r.(?) p.(Arg285Trp)
?/. - c.1019C>T r.(?) p.(Ala340Val)
?/. - c.1019C>T r.(?) p.(Ala340Val)
+/. - c.1129C>T r.(?) p.(Arg377*)
-?/. - c.1134+9A>G r.(=) p.(=)
-?/. - c.1137T>C r.(?) p.(Leu379=)
-?/. - c.1164C>T r.(?) p.(Tyr388=)
?/. - c.1234G>T r.(?) p.(Ala412Ser)
-?/. - c.1326G>A r.(?) p.(Ser442=)
+?/. 9 c.1414C>T r.(?) p.(Arg472Ter)
+/. - c.1414C>T r.(?) p.(Arg472*)
+/. - c.1532C>T r.(?) p.(Thr511Met)
-/. - c.1692C>T r.(?) p.(Asn564=)
-?/. - c.1739A>G r.(?) p.(Asn580Ser)
-?/. - c.1768+8G>A r.(=) p.(=)
?/. - c.1817A>G r.(?) p.(Tyr606Cys)
+/. - c.1840C>T r.(?) p.(Arg614*)
?/. - c.1869C>T r.(=) p.(=)
-?/. - c.1899G>A r.(?) p.(Ala633=)
+/. - c.1908del r.(?) p.(Pro637Argfs*9)
?/. - c.1958C>T r.(?) p.(Thr653Met)
+?/. - c.1982del r.(?) p.(Gly661ValfsTer21)
?/. - c.2031C>G r.(?) p.(Asn677Lys)
?/. - c.2115-2849G>A r.(=) p.(=)
+/. - c.2271del r.(?) p.(Thr758LeufsTer10)
-?/. - c.2341C>A r.(?) p.(Gln781Lys)
-?/. - c.2475G>A r.(?) p.(Arg825=)
+/. - c.2491C>T r.(?) p.(Arg831*)
-/. - c.2557-13T>A r.(=) p.(=)
-/. - c.2557-13T>A r.(=) p.(=)
?/. - c.2597C>T r.(?) p.(Pro866Leu)
-?/. - c.2658G>A r.(?) p.(Pro886=)
?/. - c.2671A>C r.(?) p.(Thr891Pro)
-?/. - c.2700-4G>T r.spl? p.?
+/. 18i_23_ c.(2699+1_2700-1)_(*1480221_*1487992)del r.? p.?
-/. - c.2799C>T r.(?) p.(Gly933=)
?/. - c.2800G>A r.(?) p.(Glu934Lys)
-?/. - c.2811-4G>A r.spl? p.?
?/. - c.2819T>C r.(?) p.(Ile940Thr)
?/. - c.2827G>C r.(?) p.(Asp943His)
+?/. - c.3034C>T r.(?) p.(Gln1012*)
+?/. - c.3056-2A>G r.spl? p.?
?/. - c.3098C>T r.(?) p.(Ala1033Val)
-?/. - c.3125G>A r.(?) p.(Arg1042His)
?/. - c.3148C>T r.(?) p.(Arg1050Trp)
?/. - c.3148C>T r.(?) p.(Arg1050Trp)
?/. - c.3211G>A r.(?) p.(Gly1071Ser)
+?/. - c.3279+1G>A r.spl? p.?
-?/. - c.3411C>A r.(?) p.(Pro1137=)
?/. - c.3414T>G r.(?) p.(Ser1138Arg)
+/. - c.3436del r.(3436del) p.(Ala1146Argfs*86)
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