Transcript #00025898 (NM_152564.4, VPS13B gene)

Transcript name transcript variant 1
Gene name VPS13B (vacuolar protein sorting 13 homolog B (yeast))
Chromosome 8
Transcript - NCBI ID NM_152564.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_689777.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2024-01-25 15:54:45 +01:00 (CET)
Date last edited N/A


Variants

687 entries on 7 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.8A>T r.(?) p.(Glu3Val)
-/. - c.147+90A>G r.(=) p.(=)
-/. - c.147+112T>C r.(=) p.(=)
?/. - c.148-8608G>C r.(=) p.(=)
?/. - c.148-16T>A r.spl? p.?
-/. - c.174A>G r.(?) p.(Leu58=)
?/. - c.203A>G r.(?) p.(His68Arg)
+?/. - c.291+1G>A r.spl? p.?
-?/. - c.292-3T>C r.spl? p.?
?/. - c.292C>T r.(?) p.(Arg98Trp)
?/. - c.328C>T r.(?) p.(Arg110Cys)
-?/. - c.358A>G r.(?) p.(Ile120Val)
?/. - c.365C>T r.(?) p.(Pro122Leu)
+/. - c.412+3161_580+208del r.(?) p.(Gly138_Ser193del)
+?/. - c.436C>T r.(?) p.(Arg146Ter)
+?/. - c.468_471del r.(?) p.(Asn157Serfs*3)
?/. - c.505C>A r.(?) p.(Leu169Ile)
-?/. - c.560G>A r.(?) p.(Arg187His)
?/. - c.560G>A r.(?) p.(Arg187His)
?/. - c.560G>A r.(?) p.(Arg187His)
?/. - c.565T>C r.(?) p.(Phe189Leu)
?/. - c.565T>C r.(?) p.(Phe189Leu)
-/. - c.581-17T>C r.(=) p.(=)
-?/. - c.581-10T>C r.(=) p.(=)
-?/. - c.581-10T>C r.(=) p.(=)
-?/. - c.581-8C>T r.(=) p.(=)
?/. - c.584C>G r.(?) p.(Thr195Ser)
?/. - c.584C>G r.(?) p.(Thr195Ser)
?/. - c.584C>G r.(?) p.(Thr195Ser)
?/. - c.584C>G r.(?) p.(Thr195Ser)
-?/. - c.690C>T r.(?) p.(Tyr230=)
?/. - c.709C>T r.(?) p.(Arg237Cys)
-?/. - c.750A>G r.(?) p.(Pro250=)
-/. - c.762+19del r.(=) p.(=)
-/. - c.763-89C>A r.(=) p.(=)
-/. - c.763-78C>G r.(=) p.(=)
?/. - c.796A>G r.(?) p.(Ile266Val)
?/. - c.857A>G r.(?) p.(Tyr286Cys)
-?/. - c.874T>G r.(?) p.(Phe292Val)
?/. - c.885C>T r.(?) p.(Gly295=)
+/. - c.901_904del r.(?) p.(Thr301ValfsTer7)
-?/. - c.921G>A r.(?) p.(Met307Ile)
+?/. - c.938-8A>G r.(=) p.(=)
+?/. - c.979C>T r.(?) p.(Gln327*)
+?/. - c.979C>T r.(?) p.(Gln327*)
-?/. - c.983A>G r.(?) p.(His328Arg)
-?/. - c.983A>G r.(?) p.(His328Arg)
-?/. - c.983A>G r.(?) p.(His328Arg)
?/. - c.1000T>C r.(?) p.(Tyr334His)
-?/. - c.1041A>G r.(?) p.(Ser347=)
-?/. - c.1041A>G r.(?) p.(Ser347=)
-?/. - c.1081G>A r.(?) p.(Asp361Asn)
-?/. - c.1082A>G r.(?) p.(Asp361Gly)
?/. - c.1108G>C r.(?) p.(Asp370His)
-/. - c.1206+33T>G r.(=) p.(=)
-/. - c.1206+33T>G r.(=) p.(=)
-/. - c.1206+33T>G r.(=) p.(=)
?/. - c.1248G>T r.(?) p.(Gln416His)
?/. - c.1248G>T r.(?) p.(Gln416His)
+?/. - c.1248G>T r.(?) p.(Gln416His)
?/. - c.1248G>T r.(?) p.(Gln416His)
?/. - c.1248G>T r.(?) p.(Gln416His)
-?/. - c.1293T>G r.(?) p.(Thr431=)
-?/. - c.1293T>G r.(?) p.(Thr431=)
-/. - c.1293T>G r.(?) p.(Thr431=)
-?/. - c.1302+12A>G r.(=) p.(=)
-?/. - c.1303-9G>A r.(=) p.(=)
-?/. - c.1303-9G>A r.(=) p.(=)
-?/. - c.1303-9G>A r.(=) p.(=)
?/. - c.1343G>A r.(?) p.(Gly448Glu)
?/. - c.1354T>G r.(?) p.(Cys452Gly)
-?/. - c.1440C>T r.(?) p.(Phe480=)
-?/. - c.1440C>T r.(?) p.(Phe480=)
+?/. - c.1443_1444del r.(?) p.(Ile481Metfs*3)
-?/. - c.1463C>T r.(?) p.(Thr488Met)
-?/. - c.1463C>T r.(?) p.(Thr488Met)
?/. - c.1520A>G r.(?) p.(Asn507Ser)
?/. - c.1528C>T r.(?) p.(Arg510Cys)
-/. - c.1536A>G r.(?) p.(Glu512=)
-?/. - c.1552A>T r.(?) p.(Thr518Ser)
-?/. - c.1552A>T r.(?) p.(Thr518Ser)
?/. - c.1559A>G r.(?) p.(His520Arg)
?/. - c.1559A>G r.(?) p.(His520Arg)
?/. - c.1559A>G r.(?) p.(His520Arg)
+?/. - c.1563G>A r.(=) p.(=)
-?/. - c.1639A>G r.(?) p.(Thr547Ala)
-/. - c.1656C>A r.(?) p.(Ser552=)
?/. - c.1700G>A r.(?) p.(Gly567Glu)
?/. - c.1768G>A r.(?) p.(Ala590Thr)
-?/. - c.1768G>A r.(?) p.(Ala590Thr)
-?/. - c.1768G>A r.(?) p.(Ala590Thr)
-/. - c.1782T>C r.(?) p.(Ile594=)
-/. - c.1786A>C r.(?) p.(Lys596Gln)
-?/. - c.1832G>A r.(?) p.(Arg611Lys)
-?/. - c.1832G>A r.(?) p.(Arg611Lys)
-?/. - c.1832G>A r.(?) p.(Arg611Lys)
-?/. - c.1832G>A r.(?) p.(Arg611Lys)
-?/. - c.1843+10T>C r.(=) p.(=)
-/. - c.1843+16A>G r.(=) p.(=)
-?/. - c.1864A>G r.(?) p.(Thr622Ala)
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