Primary Site >> Stomach Cancer
Gene >> NINL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25505010:25505010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586A>G |
| AA Mutation | p.Thr196Ala(p.T196A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25461607:25461607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3611A>G |
| AA Mutation | p.Glu1204Gly(p.E1204G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25453540:25453540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200080729 |
| CDS Mutation | c.4060G>A |
| AA Mutation | p.Ala1354Thr(p.A1354T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25498275:25498275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1104G>A |
| AA Mutation | p.Met368Ile(p.M368I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476742:25476742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755156661 |
| CDS Mutation | c.2549G>A |
| AA Mutation | p.Arg850His(p.R850H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476083:25476083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763755978 |
| CDS Mutation | c.3208C>T |
| AA Mutation | p.Arg1070Trp(p.R1070W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476088:25476088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3203T>C |
| AA Mutation | p.Val1068Ala(p.V1068A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25500965:25500965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.907G>A |
| AA Mutation | p.Val303Met(p.V303M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25512982:25512982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302A>C |
| AA Mutation | p.Lys101Thr(p.K101T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25512908:25512908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369056472 |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Arg126Cys(p.R126C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25453592:25453592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4008G>C |
| AA Mutation | p.Glu1336Asp(p.E1336D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476233:25476233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3058G>T |
| AA Mutation | p.Gly1020Trp(p.G1020W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476667:25476667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2624C>G |
| AA Mutation | p.Ala875Gly(p.A875G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476833:25476833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762729377 |
| CDS Mutation | c.2458C>T |
| AA Mutation | p.Pro820Ser(p.P820S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476569:25476569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2722C>T |
| AA Mutation | p.Arg908Cys(p.R908C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476047:25476047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780653118 |
| CDS Mutation | c.3244G>A |
| AA Mutation | p.Asp1082Asn(p.D1082N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25481977:25481977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763077917 |
| CDS Mutation | c.1801G>A |
| AA Mutation | p.Gly601Ser(p.G601S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25500944:25500944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928C>T |
| AA Mutation | p.Arg310Cys(p.R310C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476424:25476424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777373823 |
| CDS Mutation | c.2867G>A |
| AA Mutation | p.Arg956Gln(p.R956Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25482088:25482088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533440102 |
| CDS Mutation | c.1690C>T |
| AA Mutation | p.Arg564Cys(p.R564C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278886 |
| Start | 25481994:25481994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767236224 |
| CDS Mutation | c.1784G>A |
| AA Mutation | p.Arg595Gln(p.R595Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25479195:25479195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148406486 |
| CDS Mutation | c.1929C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25526423:25526423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374578020 |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25491437:25491437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476048:25476048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144098143 |
| CDS Mutation | c.3243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25517808:25517808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.222G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476894:25476894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2397C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25476612:25476612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763227385 |
| CDS Mutation | c.2679C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278886 |
| Start | 25504012:25504012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146594321 |
| CDS Mutation | c.801C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000278886 |
| Start | 25504968:25504968(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.628delG |
| AA Mutation | p.Val210TrpfsTer7(p.V210Wfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000278886 |
| Start | 25453546:25453546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752565890 |
| CDS Mutation | c.4054C>T |
| AA Mutation | p.Arg1352Ter(p.R1352*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |