Primary Site >> Stomach Cancer
Gene >> NOS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117272512:117272512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1712C>T |
| AA Mutation | p.Ala571Val(p.A571V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117286150:117286150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Arg415Gln(p.R415Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234756:117234756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3044G>A |
| AA Mutation | p.Arg1015Gln(p.R1015Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117286151:117286151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243C>T |
| AA Mutation | p.Arg415Trp(p.R415W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117218064:117218064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4271G>A |
| AA Mutation | p.Ser1424Asn(p.S1424N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117268138:117268138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1846G>A |
| AA Mutation | p.Ala616Thr(p.A616T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234586:117234586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3214G>C |
| AA Mutation | p.Glu1072Gln(p.E1072Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330354:117330354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.716A>G |
| AA Mutation | p.Gln239Arg(p.Q239R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117290369:117290369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763590379 |
| CDS Mutation | c.910C>T |
| AA Mutation | p.Arg304Cys(p.R304C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117259076:117259076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2422C>A |
| AA Mutation | p.Leu808Ile(p.L808I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117222824:117222824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199524143 |
| CDS Mutation | c.3866G>A |
| AA Mutation | p.Arg1289Gln(p.R1289Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234726:117234726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3074A>T |
| AA Mutation | p.Asn1025Ile(p.N1025I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117220202:117220202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781077618 |
| CDS Mutation | c.4043G>A |
| AA Mutation | p.Gly1348Glu(p.G1348E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117331034:117331034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569264110 |
| CDS Mutation | c.36G>T |
| AA Mutation | p.Gln12His(p.Q12H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117259036:117259036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2462A>G |
| AA Mutation | p.Glu821Gly(p.E821G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117268123:117268123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1861T>G |
| AA Mutation | p.Leu621Val(p.L621V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117286162:117286162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1232A>C |
| AA Mutation | p.Lys411Thr(p.K411T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117290303:117290303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757597537 |
| CDS Mutation | c.976A>G |
| AA Mutation | p.Thr326Ala(p.T326A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330933:117330933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.137T>G |
| AA Mutation | p.Leu46Arg(p.L46R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234624:117234624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56266548 |
| CDS Mutation | c.3176C>T |
| AA Mutation | p.Ala1059Val(p.A1059V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117280786:117280786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1463C>T |
| AA Mutation | p.Ala488Val(p.A488V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117222791:117222791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3899A>C |
| AA Mutation | p.Glu1300Ala(p.E1300A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117227461:117227461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3586A>G |
| AA Mutation | p.Thr1196Ala(p.T1196A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117280832:117280832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371044828 |
| CDS Mutation | c.1417G>A |
| AA Mutation | p.Gly473Ser(p.G473S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117260520:117260520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150227193 |
| CDS Mutation | c.2312C>T |
| AA Mutation | p.Ser771Leu(p.S771L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117247357:117247357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2814G>T |
| AA Mutation | p.Lys938Asn(p.K938N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117286138:117286138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1256G>A |
| AA Mutation | p.Arg419His(p.R419H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117227578:117227578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3469G>A |
| AA Mutation | p.Glu1157Lys(p.E1157K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117232093:117232093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3274C>T |
| AA Mutation | p.Pro1092Ser(p.P1092S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234739:117234739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375069851 |
| CDS Mutation | c.3061C>T |
| AA Mutation | p.Arg1021Cys(p.R1021C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317775 |
| Start | 117268125:117268125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1859A>G |
| AA Mutation | p.Asn620Ser(p.N620S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117226745:117226745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778538175 |
| CDS Mutation | c.3642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330581:117330581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375672027 |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234620:117234620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3180G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117247477:117247477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375782081 |
| CDS Mutation | c.2694C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117285327:117285327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753948003 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117227627:117227627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747681671 |
| CDS Mutation | c.3420C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117243319:117243319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540391266 |
| CDS Mutation | c.2940C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330983:117330983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.87A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330953:117330953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.117G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117220153:117220153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4092C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117234656:117234656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374883833 |
| CDS Mutation | c.3144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117288139:117288139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117272508:117272508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749731239 |
| CDS Mutation | c.1716G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317775 |
| Start | 117277970:117277970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1653C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317775 |
| Start | 117243389:117243389(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2870delA |
| AA Mutation | p.Lys957ArgfsTer93(p.K957Rfs*93) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317775 |
| Start | 117265425:117265425(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768009637 |
| CDS Mutation | c.2027delG |
| AA Mutation | p.Gly676AlafsTer64(p.G676Afs*64) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317775 |
| Start | 117330530:117330530(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.540delC |
| AA Mutation | p.Arg181GlyfsTer29(p.R181Gfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000317775 |
| Start | 117330985:117330985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.85G>T |
| AA Mutation | p.Gly29Ter(p.G29*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000317775 |
| Start | 117253741:117253741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2545C>T |
| AA Mutation | p.Arg849Ter(p.R849*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000317775 |
| Start | 117218155:117218155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751893456 |
| CDS Mutation | c.4180C>T |
| AA Mutation | p.Arg1394Ter(p.R1394*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |