All transcript variants in gene NAMPT

Information The variants shown are described using the NM_005746.2 transcript reference sequence.

67 entries on 1 page. Showing entries 1 - 67.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-51G>T r.(=) p.(=) g.105925381C>A Copied from the Exome Variant Server NAMPT_000067 4/12846 0/8502 4/4344
?/? c.-13C>T r.(=) p.(=) g.105925343G>A Copied from the Exome Variant Server NAMPT_000066 1/12908 1/8542 0/4366
?/? c.48C>T r.(=) p.(=) g.105925283G>A Copied from the Exome Variant Server NAMPT_000065 1/12872 1/8536 0/4336
?/? c.57+32A>T r.(=) p.(=) g.105925242T>A Copied from the Exome Variant Server NAMPT_000064 39/11798 36/7882 3/3916
?/? c.58-51T>A r.(=) p.(=) g.105917676A>T Copied from the Exome Variant Server NAMPT_000063 2/12980 0/8588 2/4392
?/? c.72A>G r.(=) p.(=) g.105917611T>C Copied from the Exome Variant Server NAMPT_000062 1/12990 0/8588 1/4402
?/? c.150G>A r.(=) p.(=) g.105917533C>T Copied from the Exome Variant Server NAMPT_000061 1/12990 1/8586 0/4404
?/? c.152A>G r.(?) p.(Lys51Arg) g.105917531T>C Copied from the Exome Variant Server NAMPT_000060 1/12990 0/8586 1/4404
?/? c.196C>G r.(?) p.(Leu66Val) g.105917487G>C Copied from the Exome Variant Server NAMPT_000059 1/12994 0/8590 1/4404
?/? c.214+47C>T r.(=) p.(=) g.105917422G>A Copied from the Exome Variant Server NAMPT_000058 2/12974 1/8578 1/4396
?/? c.215-37C>A r.(=) p.(=) g.105915532G>T Copied from the Exome Variant Server NAMPT_000057 2/12998 2/8598 0/4400
?/? c.215-34T>G r.(=) p.(=) g.105915529A>C Copied from the Exome Variant Server NAMPT_000056 1/13000 1/8598 0/4402
?/? c.263A>G r.(?) p.(Lys88Arg) g.105915447T>C Copied from the Exome Variant Server NAMPT_000055 1/13004 0/8600 1/4404
?/? c.281A>G r.(?) p.(Asp94Gly) g.105915429T>C Copied from the Exome Variant Server NAMPT_000054 1/13004 1/8600 0/4404
?/? c.318+39_318+40insT r.(=) p.(=) g.105915352_105915353insA Copied from the Exome Variant Server NAMPT_000053 2/12512 0/8252 2/4260
?/? c.318+44del r.(=) p.(=) g.105915348del Copied from the Exome Variant Server NAMPT_000052 1/12514 1/8254 0/4260
?/? c.319-51G>C r.(=) p.(=) g.105913155C>G Copied from the Exome Variant Server NAMPT_000050 395/12996 157/8594 238/4402
?/? c.319-39A>G r.(=) p.(=) g.105913143T>C Copied from the Exome Variant Server NAMPT_000051 2/13000 0/8594 2/4406
?/? c.319-37C>G r.(=) p.(=) g.105913141G>C Copied from the Exome Variant Server NAMPT_000049 1/13000 1/8594 0/4406
?/? c.332A>G r.(?) p.(His111Arg) g.105913091T>C Copied from the Exome Variant Server NAMPT_000048 1/13006 1/8600 0/4406
?/? c.340A>G r.(?) p.(Ile114Val) g.105913083T>C Copied from the Exome Variant Server NAMPT_000047 1/13006 0/8600 1/4406
?/? c.417A>G r.(=) p.(=) g.105913006T>C Copied from the Exome Variant Server NAMPT_000046 1/13006 1/8600 0/4406
?/? c.447+444A>G r.(=) p.(=) g.105912532T>C Copied from the Exome Variant Server NAMPT_000045 3/5644 3/3926 0/1718
?/? c.606+15C>T r.(=) p.(=) g.105909585G>A Copied from the Exome Variant Server NAMPT_000044 1/13006 1/8600 0/4406
?/? c.607-51T>G r.(=) p.(=) g.105909097A>C Copied from the Exome Variant Server NAMPT_000043 5/12968 5/8588 0/4380
?/? c.607-47G>A r.(=) p.(=) g.105909093C>T Copied from the Exome Variant Server NAMPT_000042 3/12986 3/8594 0/4392
?/? c.607-33G>A r.(=) p.(=) g.105909079C>T Copied from the Exome Variant Server NAMPT_000041 1/12998 0/8598 1/4400
?/? c.698C>T r.(?) p.(Thr233Met) g.105908955G>A Copied from the Exome Variant Server NAMPT_000040 1/13006 1/8600 0/4406
?/? c.743+49T>A r.(=) p.(=) g.105908861A>T Copied from the Exome Variant Server NAMPT_000039 5/12964 0/8586 5/4378
?/? c.744-50T>C r.(=) p.(=) g.105904113A>G Copied from the Exome Variant Server NAMPT_000038 1/12986 0/8592 1/4394
?/? c.744-27A>C r.(=) p.(=) g.105904090T>G Copied from the Exome Variant Server NAMPT_000037 1/13000 0/8596 1/4404
?/? c.744-20_744-19del r.(=) p.(=) g.105904082_105904083del Copied from the Exome Variant Server NAMPT_000036 1/12510 1/8250 0/4260
?/? c.744-5del r.spl? p.? g.105904068del Copied from the Exome Variant Server NAMPT_000035 42/12508 22/8250 20/4258
?/? c.744-5dup r.spl? p.? g.105904068dup Copied from the Exome Variant Server NAMPT_000034 21/12508 13/8250 8/4258
?/? c.903A>G r.(=) p.(=) g.105903904T>C Copied from the Exome Variant Server NAMPT_000033 7864/13002 5374/8596 2490/4406
?/? c.912A>G r.(=) p.(=) g.105903895T>C Copied from the Exome Variant Server NAMPT_000032 3/13002 2/8596 1/4406
?/? c.969+22T>C r.(=) p.(=) g.105903816A>G Copied from the Exome Variant Server NAMPT_000031 4/13004 3/8598 1/4406
?/? c.969+36C>T r.(=) p.(=) g.105903802G>A Copied from the Exome Variant Server NAMPT_000030 1/13004 1/8598 0/4406
?/? c.969+49C>G r.(=) p.(=) g.105903789G>C Copied from the Exome Variant Server NAMPT_000029 127/12996 116/8592 11/4404
?/? c.970-31A>C r.(=) p.(=) g.105902184T>G Copied from the Exome Variant Server NAMPT_000028 1/12992 0/8586 1/4406
?/? c.970-30T>C r.(=) p.(=) g.105902183A>G Copied from the Exome Variant Server NAMPT_000027 3/12994 3/8588 0/4406
?/? c.999T>C r.(=) p.(=) g.105902124A>G Copied from the Exome Variant Server NAMPT_000026 36/12998 29/8592 7/4406
?/? c.1089+27A>G r.(=) p.(=) g.105902007T>C Copied from the Exome Variant Server NAMPT_000025 4/12984 4/8584 0/4400
?/? c.1089+42T>C r.(=) p.(=) g.105901992A>G Copied from the Exome Variant Server NAMPT_000024 1/12912 0/8558 1/4354
?/? c.1089+47_1089+50del r.(=) p.(=) g.105901984_105901987del Copied from the Exome Variant Server NAMPT_000023 10/12364 0/8184 10/4180
?/? c.1089+52T>C r.(=) p.(=) g.105901982A>G Copied from the Exome Variant Server NAMPT_000022 112/5728 0/3980 112/1748
?/? c.1090-36G>T r.(=) p.(=) g.105894986C>A Copied from the Exome Variant Server NAMPT_000021 2/13000 0/8594 2/4406
?/? c.1090-26G>T r.(=) p.(=) g.105894976C>A Copied from the Exome Variant Server NAMPT_000020 3/13002 2/8596 1/4406
?/? c.1090-21T>G r.(=) p.(=) g.105894971A>C Copied from the Exome Variant Server NAMPT_000019 72/13002 0/8596 72/4406
?/? c.1090-9A>C r.(=) p.(=) g.105894959T>G Copied from the Exome Variant Server NAMPT_000018 7/13004 5/8598 2/4406
?/? c.1159C>T r.(=) p.(=) g.105894881G>A Copied from the Exome Variant Server NAMPT_000017 1/13006 0/8600 1/4406
?/? c.1173_1174del r.(?) p.(Asp393Serfs*9) g.105894866_105894867del Copied from the Exome Variant Server NAMPT_000016 1/12518 0/8254 1/4264
?/? c.1230+44G>A r.(=) p.(=) g.105894766C>T Copied from the Exome Variant Server NAMPT_000015 1/13004 0/8598 1/4406
?/? c.1304C>T r.(?) p.(Thr435Met) g.105893524G>A Copied from the Exome Variant Server NAMPT_000014 2/13006 0/8600 2/4406
?/? c.1320T>C r.(=) p.(=) g.105893508A>G Copied from the Exome Variant Server NAMPT_000013 9/13006 0/8600 9/4406
?/? c.1328T>C r.(?) p.(Leu443Pro) g.105893500A>G Copied from the Exome Variant Server NAMPT_000012 1/13006 1/8600 0/4406
?/? c.1358A>G r.(?) p.(Tyr453Cys) g.105893470T>C Copied from the Exome Variant Server NAMPT_000011 2/13006 2/8600 0/4406
?/? c.1365G>A r.(=) p.(=) g.105893463C>T Copied from the Exome Variant Server NAMPT_000010 2/13006 2/8600 0/4406
?/? c.1365+7A>G r.(=) p.(=) g.105893456T>C Copied from the Exome Variant Server NAMPT_000009 2/13006 2/8600 0/4406
?/? c.1365+41G>T r.(=) p.(=) g.105893422C>A Copied from the Exome Variant Server NAMPT_000008 1/13006 1/8600 0/4406
?/? c.1366-49G>T r.(=) p.(=) g.105891688C>A Copied from the Exome Variant Server NAMPT_000007 1/12988 1/8590 0/4398
?/? c.1366-47A>G r.(=) p.(=) g.105891686T>C Copied from the Exome Variant Server NAMPT_000006 1/12988 1/8590 0/4398
?/? c.1366-33T>G r.(=) p.(=) g.105891672A>C Copied from the Exome Variant Server NAMPT_000005 34/12990 1/8590 33/4400
?/? c.1366-22C>A r.(=) p.(=) g.105891661G>T Copied from the Exome Variant Server NAMPT_000004 1/12996 0/8592 1/4404
?/? c.1366-8T>C r.(=) p.(=) g.105891647A>G Copied from the Exome Variant Server NAMPT_000003 54/13002 51/8596 3/4406
?/? c.1424A>C r.(?) p.(Glu475Ala) g.105891581T>G Copied from the Exome Variant Server NAMPT_000002 6/12994 0/8588 6/4406
?/? c.*2C>T r.(=) p.(=) g.105891527G>A Copied from the Exome Variant Server NAMPT_000001 1/13000 1/8596 0/4404
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