Primary Site >> Stomach Cancer
Gene >> MYH7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23418385:23418385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397516198 |
| CDS Mutation | c.3994G>A |
| AA Mutation | p.Ala1332Thr(p.A1332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23429255:23429255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730880868 |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Val411Ile(p.V411I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23424974:23424974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2474A>T |
| AA Mutation | p.Lys825Met(p.K825M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23432744:23432744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199637885 |
| CDS Mutation | c.397G>A |
| AA Mutation | p.Val133Met(p.V133M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23418234:23418234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727504325 |
| CDS Mutation | c.4145G>A |
| AA Mutation | p.Arg1382Gln(p.R1382Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416286:23416286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4671G>T |
| AA Mutation | p.Lys1557Asn(p.K1557N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000355349 |
| Start | 23424770:23424770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727503254 |
| CDS Mutation | c.2678C>T |
| AA Mutation | p.Ala893Val(p.A893V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23427792:23427792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730880878 |
| CDS Mutation | c.1681G>A |
| AA Mutation | p.Ala561Thr(p.A561T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23415104:23415104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5450C>T |
| AA Mutation | p.Ala1817Val(p.A1817V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416276:23416276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4681G>A |
| AA Mutation | p.Ala1561Thr(p.A1561T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23428990:23428990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1372G>A |
| AA Mutation | p.Gly458Arg(p.G458R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23420129:23420129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs786205355 |
| CDS Mutation | c.3442G>A |
| AA Mutation | p.Glu1148Lys(p.E1148K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000355349 |
| Start | 23433532:23433532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.201G>T |
| AA Mutation | p.Lys67Asn(p.K67N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23429004:23429004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397516101 |
| CDS Mutation | c.1358G>A |
| AA Mutation | p.Arg453His(p.R453H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23419937:23419937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3634C>T |
| AA Mutation | p.Arg1212Trp(p.R1212W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23418274:23418274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4105G>A |
| AA Mutation | p.Ala1369Thr(p.A1369T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417180:23417180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4492T>G |
| AA Mutation | p.Phe1498Val(p.F1498V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23419957:23419957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3614A>C |
| AA Mutation | p.Glu1205Ala(p.E1205A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23419558:23419558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755386220 |
| CDS Mutation | c.3778C>T |
| AA Mutation | p.Arg1260Trp(p.R1260W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23425358:23425358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727503258 |
| CDS Mutation | c.2347C>T |
| AA Mutation | p.Arg783Cys(p.R783C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416057:23416057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397516232 |
| CDS Mutation | c.4900C>T |
| AA Mutation | p.Arg1634Cys(p.R1634C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23427773:23427773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377491278 |
| CDS Mutation | c.1700G>A |
| AA Mutation | p.Arg567His(p.R567H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23415691:23415691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5095C>T |
| AA Mutation | p.Arg1699Trp(p.R1699W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23433666:23433666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730880828 |
| CDS Mutation | c.67C>T |
| AA Mutation | p.Arg23Trp(p.R23W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23415652:23415652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913650 |
| CDS Mutation | c.5134C>T |
| AA Mutation | p.Arg1712Trp(p.R1712W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23431774:23431774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.626A>G |
| AA Mutation | p.Gln209Arg(p.Q209R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23423921:23423921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2908G>A |
| AA Mutation | p.Ala970Thr(p.A970T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23418327:23418327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370403289 |
| CDS Mutation | c.4052C>T |
| AA Mutation | p.Thr1351Met(p.T1351M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416051:23416051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4906G>A |
| AA Mutation | p.Ala1636Thr(p.A1636T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23424842:23424842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202141173 |
| CDS Mutation | c.2606G>A |
| AA Mutation | p.Arg869His(p.R869H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23428643:23428643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1435A>G |
| AA Mutation | p.Asn479Asp(p.N479D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417597:23417597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4259G>T |
| AA Mutation | p.Arg1420Leu(p.R1420L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417536:23417536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772520956 |
| CDS Mutation | c.4320A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23415794:23415794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763538103 |
| CDS Mutation | c.4992C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416169:23416169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146858930 |
| CDS Mutation | c.4788G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23433556:23433556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23422254:23422254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758822596 |
| CDS Mutation | c.3171C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23429256:23429256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150885220 |
| CDS Mutation | c.1230C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23415160:23415160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777053791 |
| CDS Mutation | c.5394C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23413867:23413867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5682C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000355349 |
| Start | 23424907:23424909(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs397516155 |
| CDS Mutation | c.2539_2541delAAG |
| AA Mutation | p.Lys847del(p.K847del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |