Primary Site >> Stomach Cancer
Gene >> ADGRB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142522109:142522109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3169G>A |
| AA Mutation | p.Gly1057Ser(p.G1057S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142543431:142543431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4442A>T |
| AA Mutation | p.Asp1481Val(p.D1481V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477450:142477450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76763828 |
| CDS Mutation | c.1288C>T |
| AA Mutation | p.Arg430Trp(p.R430W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142518228:142518228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577805420 |
| CDS Mutation | c.2908G>A |
| AA Mutation | p.Val970Met(p.V970M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542009:142542009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3775C>T |
| AA Mutation | p.Pro1259Ser(p.P1259S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477200:142477200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773821198 |
| CDS Mutation | c.1144G>A |
| AA Mutation | p.Val382Met(p.V382M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142489052:142489052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751615897 |
| CDS Mutation | c.2470G>A |
| AA Mutation | p.Val824Met(p.V824M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142533417:142533417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3521C>T |
| AA Mutation | p.Ser1174Leu(p.S1174L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142543415:142543415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778880062 |
| CDS Mutation | c.4426C>T |
| AA Mutation | p.Arg1476Trp(p.R1476W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142481268:142481268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765738842 |
| CDS Mutation | c.1843C>T |
| AA Mutation | p.Arg615Trp(p.R615W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142479746:142479746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1780A>G |
| AA Mutation | p.Thr594Ala(p.T594A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142489420:142489420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613G>C |
| AA Mutation | p.Glu871Asp(p.E871D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542159:142542159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3925C>A |
| AA Mutation | p.Leu1309Ile(p.L1309I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142489400:142489400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757292289 |
| CDS Mutation | c.2593C>T |
| AA Mutation | p.Arg865Cys(p.R865C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142533374:142533374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3478C>T |
| AA Mutation | p.Arg1160Cys(p.R1160C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477186:142477186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142533378:142533378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3482G>A |
| AA Mutation | p.Arg1161His(p.R1161H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477462:142477462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1300C>T |
| AA Mutation | p.Arg434Cys(p.R434C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542296:142542296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376053773 |
| CDS Mutation | c.4062G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142522105:142522105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142533412:142533412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745665205 |
| CDS Mutation | c.3516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477395:142477395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1233C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142489042:142489042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765764021 |
| CDS Mutation | c.2460T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142518227:142518227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556293550 |
| CDS Mutation | c.2907C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542134:142542134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371373603 |
| CDS Mutation | c.3900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542287:142542287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323289 |
| Start | 142481307:142481307(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1887delC |
| AA Mutation | p.Thr630ProfsTer15(p.T630Pfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323289 |
| Start | 142475521:142475521(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.836delG |
| AA Mutation | p.Gly279GlufsTer311(p.G279Efs*311) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000323289 |
| Start | 142481544:142481544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1963C>T |
| AA Mutation | p.Arg655Ter(p.R655*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000323289 |
| Start | 142488445:142488445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2390G>A |
| AA Mutation | p.Trp797Ter(p.W797*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477473:142477474(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772974645 |
| CDS Mutation | c.1318dupC |
| AA Mutation | p.Gln440ProfsTer8(p.Q440Pfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |