Primary Site >> Stomach Cancer
Gene >> MYO3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26168745:26168745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3145A>C |
| AA Mutation | p.Asn1049His(p.N1049H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26193255:26193255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4489C>T |
| AA Mutation | p.Arg1497Trp(p.R1497W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26016867:26016867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556G>A |
| AA Mutation | p.Val186Ile(p.V186I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26174165:26174165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745554914 |
| CDS Mutation | c.3901A>G |
| AA Mutation | p.Met1301Val(p.M1301V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26211940:26211940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4828C>T |
| AA Mutation | p.Arg1610Trp(p.R1610W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26201290:26201290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4571G>T |
| AA Mutation | p.Arg1524Ile(p.R1524I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26166167:26166167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3100G>A |
| AA Mutation | p.Gly1034Arg(p.G1034R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26193221:26193221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4455G>T |
| AA Mutation | p.Glu1485Asp(p.E1485D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 25954975:25954975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.270A>C |
| AA Mutation | p.Lys90Asn(p.K90N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26143496:26143496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2311G>A |
| AA Mutation | p.Asp771Asn(p.D771N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26174169:26174169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3905A>G |
| AA Mutation | p.Glu1302Gly(p.E1302G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 25952184:25952184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.74A>C |
| AA Mutation | p.Glu25Ala(p.E25A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265944 |
| Start | 26096478:26096478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660A>T |
| AA Mutation | p.Arg554Trp(p.R554W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26173873:26173873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3609A>C |
| AA Mutation | p.Glu1203Asp(p.E1203D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26168719:26168719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3119T>G |
| AA Mutation | p.Leu1040Arg(p.L1040R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26096668:26096668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776219381 |
| CDS Mutation | c.1762G>A |
| AA Mutation | p.Gly588Ser(p.G588S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26173894:26173894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3630A>C |
| AA Mutation | p.Glu1210Asp(p.E1210D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 26173770:26173770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3506T>C |
| AA Mutation | p.Phe1169Ser(p.F1169S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265944 |
| Start | 25954895:25954895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.190G>A |
| AA Mutation | p.Ala64Thr(p.A64T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26125486:26125486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1992A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26166121:26166121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3054C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26070326:26070326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1284T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26026449:26026449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773463362 |
| CDS Mutation | c.870T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26096444:26096444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1626A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26174266:26174266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4002G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265944 |
| Start | 26211885:26211885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4773G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265944 |
| Start | 26096401:26096401(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1588delT |
| AA Mutation | p.Tyr530ThrfsTer13(p.Y530Tfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265944 |
| Start | 26168827:26168827(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766927540 |
| CDS Mutation | c.3232delA |
| AA Mutation | p.Ile1078TyrfsTer10(p.I1078Yfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265944 |
| Start | 26173831:26173831(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3574delA |
| AA Mutation | p.Met1192Ter(p.M1192*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265944 |
| Start | 26157349:26157349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2833C>T |
| AA Mutation | p.Gln945Ter(p.Q945*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265944 |
| Start | 26174174:26174174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3910G>T |
| AA Mutation | p.Glu1304Ter(p.E1304*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265944 |
| Start | 26174446:26174446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4182T>A |
| AA Mutation | p.Tyr1394Ter(p.Y1394*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265944 |
| Start | 26193249:26193249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371876274 |
| CDS Mutation | c.4483C>T |
| AA Mutation | p.Arg1495Ter(p.R1495*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265944 |
| Start | 26176736:26176737(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772558362 |
| CDS Mutation | c.4335dupA |
| AA Mutation | p.Leu1446IlefsTer3(p.L1446Ifs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265944 |
| Start | 26070159:26070160(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1224dupT |
| AA Mutation | p.Ala409CysfsTer4(p.A409Cfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |