Primary Site >> Stomach Cancer
Gene >> CARD11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2910135:2910135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376446854 |
| CDS Mutation | c.3175G>A |
| AA Mutation | p.Gly1059Ser(p.G1059S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2939774:2939774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839A>C |
| AA Mutation | p.Asn280Thr(p.N280T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2937155:2937155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79513324 |
| CDS Mutation | c.1223G>A |
| AA Mutation | p.Arg408His(p.R408H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000396946 |
| Start | 2910051:2910051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3259A>G |
| AA Mutation | p.Arg1087Gly(p.R1087G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2939844:2939844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.769A>G |
| AA Mutation | p.Ile257Val(p.I257V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2923214:2923214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs41493047 |
| CDS Mutation | c.2060C>T |
| AA Mutation | p.Ala687Val(p.A687V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2934542:2934542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1429T>G |
| AA Mutation | p.Ser477Ala(p.S477A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2944277:2944277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619C>T |
| AA Mutation | p.Arg207Cys(p.R207C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2917331:2917331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142828146 |
| CDS Mutation | c.2662C>T |
| AA Mutation | p.Arg888Cys(p.R888C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2912206:2912206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3110T>A |
| AA Mutation | p.Ile1037Asn(p.I1037N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2913407:2913407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149857605 |
| CDS Mutation | c.2899C>T |
| AA Mutation | p.Arg967Cys(p.R967C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2937108:2937108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270C>T |
| AA Mutation | p.Arg424Trp(p.R424W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2944387:2944387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766268425 |
| CDS Mutation | c.509G>A |
| AA Mutation | p.Arg170His(p.R170H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2937156:2937156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1222C>T |
| AA Mutation | p.Arg408Cys(p.R408C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2913449:2913449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2857G>A |
| AA Mutation | p.Glu953Lys(p.E953K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2906706:2906706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3397C>T |
| AA Mutation | p.Arg1133Cys(p.R1133C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2913397:2913397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2909A>G |
| AA Mutation | p.Tyr970Cys(p.Y970C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2939754:2939754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859A>G |
| AA Mutation | p.Ile287Val(p.I287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2915357:2915357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2719G>A |
| AA Mutation | p.Glu907Lys(p.E907K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396946 |
| Start | 2924359:2924359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1814G>A |
| AA Mutation | p.Ser605Asn(p.S605N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2919581:2919581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144358235 |
| CDS Mutation | c.2301C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2934522:2934522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1449A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2944389:2944389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754649365 |
| CDS Mutation | c.507G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2906794:2906794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2912292:2912292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148497800 |
| CDS Mutation | c.3024C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2919431:2919431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141131560 |
| CDS Mutation | c.2451G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2937994:2937994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145169161 |
| CDS Mutation | c.1056G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396946 |
| Start | 2923318:2923318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1956G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396946 |
| Start | 2928689:2928689(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs764030673 |
| CDS Mutation | c.1663delC |
| AA Mutation | p.Arg555GlyfsTer45(p.R555Gfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396946 |
| Start | 2923220:2923220(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2054delG |
| AA Mutation | p.Gly685AlafsTer31(p.G685Afs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396946 |
| Start | 2928688:2928689(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs762770988 |
| CDS Mutation | c.1663dupC |
| AA Mutation | p.Arg555ProfsTer38(p.R555Pfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000396946 |
| Start | 2938018:2938020(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1030_1032delAAG |
| AA Mutation | p.Lys344del(p.K344del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |