Primary Site >> Stomach Cancer
Gene >> IGSF10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453497:151453497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602C>A |
| AA Mutation | p.Pro201His(p.P201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453746:151453746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147782448 |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Arg118Gln(p.R118Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151436766:151436766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201661662 |
| CDS Mutation | c.7795G>A |
| AA Mutation | p.Asp2599Asn(p.D2599N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446503:151446503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553213263 |
| CDS Mutation | c.3478G>A |
| AA Mutation | p.Ala1160Thr(p.A1160T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443681:151443681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5266A>G |
| AA Mutation | p.Thr1756Ala(p.T1756A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446628:151446628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3353G>T |
| AA Mutation | p.Ser1118Ile(p.S1118I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151457076:151457076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274G>T |
| AA Mutation | p.Gly92Cys(p.G92C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447930:151447930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2051C>T |
| AA Mutation | p.Ser684Phe(p.S684F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151436850:151436850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763969322 |
| CDS Mutation | c.7711T>C |
| AA Mutation | p.Ser2571Pro(p.S2571P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446025:151446025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3956C>G |
| AA Mutation | p.Pro1319Arg(p.P1319R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151444982:151444982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4999T>G |
| AA Mutation | p.Phe1667Val(p.F1667V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151448853:151448853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128A>C |
| AA Mutation | p.Gln376His(p.Q376H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443516:151443516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201180015 |
| CDS Mutation | c.5431A>G |
| AA Mutation | p.Ser1811Gly(p.S1811G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446363:151446363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3618A>T |
| AA Mutation | p.Gln1206His(p.Q1206H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447835:151447835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2146A>T |
| AA Mutation | p.Ser716Cys(p.S716C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447871:151447871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2110A>G |
| AA Mutation | p.Met704Val(p.M704V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151448841:151448841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1140G>C |
| AA Mutation | p.Leu380Phe(p.L380F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151437608:151437608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6953A>G |
| AA Mutation | p.Glu2318Gly(p.E2318G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151437655:151437655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6906T>A |
| AA Mutation | p.Asn2302Lys(p.N2302K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447796:151447796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372971163 |
| CDS Mutation | c.2185C>T |
| AA Mutation | p.Arg729Cys(p.R729C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453724:151453724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375T>A |
| AA Mutation | p.Phe125Leu(p.F125L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447775:151447775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374899455 |
| CDS Mutation | c.2206C>T |
| AA Mutation | p.Arg736Cys(p.R736C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151437395:151437395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7166T>C |
| AA Mutation | p.Leu2389Pro(p.L2389P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151444993:151444993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4988A>C |
| AA Mutation | p.Asn1663Thr(p.N1663T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151445034:151445034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4947G>T |
| AA Mutation | p.Arg1649Ser(p.R1649S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446686:151446686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3295T>C |
| AA Mutation | p.Ser1099Pro(p.S1099P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443261:151443261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5686T>G |
| AA Mutation | p.Leu1896Val(p.L1896V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151436708:151436708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376416108 |
| CDS Mutation | c.7853C>T |
| AA Mutation | p.Thr2618Met(p.T2618M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443194:151443194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5753T>C |
| AA Mutation | p.Ile1918Thr(p.I1918T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443695:151443695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768170569 |
| CDS Mutation | c.5252G>A |
| AA Mutation | p.Arg1751His(p.R1751H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151445213:151445213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4768C>T |
| AA Mutation | p.Pro1590Ser(p.P1590S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151445763:151445763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4218C>A |
| AA Mutation | p.Ser1406Arg(p.S1406R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453717:151453717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.382C>A |
| AA Mutation | p.Leu128Ile(p.L128I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453653:151453653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.446T>C |
| AA Mutation | p.Phe149Ser(p.F149S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443248:151443248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5699G>A |
| AA Mutation | p.Gly1900Glu(p.G1900E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151438447:151438447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6114C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446888:151446888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3093G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151458593:151458593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755271534 |
| CDS Mutation | c.117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447704:151447704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2277G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151448090:151448090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1891A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151445706:151445706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151443670:151443670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200610854 |
| CDS Mutation | c.5277C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151445277:151445277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4704T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151437274:151437274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7287C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151437760:151437760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6801A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282466 |
| Start | 151458542:151458542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775388305 |
| CDS Mutation | c.168G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446921:151446921(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3060delG |
| AA Mutation | p.Arg1021GlyfsTer41(p.R1021Gfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151438364:151438364(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6197delC |
| AA Mutation | p.Pro2066GlnfsTer14(p.P2066Qfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151448384:151448384(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1597delA |
| AA Mutation | p.Ser533ValfsTer20(p.S533Vfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446576:151446576(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3405delA |
| AA Mutation | p.Val1136Ter(p.V1136*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151453765:151453765(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.334delA |
| AA Mutation | p.Met112Ter(p.M112*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151447639:151447639(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2342delC |
| AA Mutation | p.Pro781GlnfsTer34(p.P781Qfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000282466 |
| Start | 151447667:151447667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148376549 |
| CDS Mutation | c.2314C>T |
| AA Mutation | p.Arg772Ter(p.R772*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000282466 |
| Start | 151436835:151436835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7726G>T |
| AA Mutation | p.Glu2576Ter(p.E2576*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151448013:151448014(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1967dupT |
| AA Mutation | p.Leu656PhefsTer18(p.L656Ffs*18) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282466 |
| Start | 151446292:151446293(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs758196369 |
| CDS Mutation | c.3688dupA |
| AA Mutation | p.Ser1230LysfsTer8(p.S1230Kfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |