Primary Site >> Stomach Cancer
Gene >> MYH6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400767:23400767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1352A>T |
| AA Mutation | p.Lys451Met(p.K451M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384708:23384708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5299A>G |
| AA Mutation | p.Met1767Val(p.M1767V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23405677:23405677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295C>T |
| AA Mutation | p.Pro99Ser(p.P99S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23388899:23388899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4135A>G |
| AA Mutation | p.Thr1379Ala(p.T1379A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23390214:23390214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765797952 |
| CDS Mutation | c.3575C>T |
| AA Mutation | p.Ala1192Val(p.A1192V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23386016:23386016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5075C>T |
| AA Mutation | p.Ala1692Val(p.A1692V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384543:23384543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5464C>T |
| AA Mutation | p.Arg1822Trp(p.R1822W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23407030:23407030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.194A>C |
| AA Mutation | p.Asn65Thr(p.N65T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23388865:23388865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4169A>G |
| AA Mutation | p.Glu1390Gly(p.E1390G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23398892:23398892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769103956 |
| CDS Mutation | c.1727C>T |
| AA Mutation | p.Ala576Val(p.A576V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400851:23400851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1268A>G |
| AA Mutation | p.Tyr423Cys(p.Y423C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23404377:23404377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.654G>T |
| AA Mutation | p.Glu218Asp(p.E218D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23385989:23385989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762103586 |
| CDS Mutation | c.5102G>A |
| AA Mutation | p.Arg1701Gln(p.R1701Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384479:23384479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5528G>T |
| AA Mutation | p.Arg1843Met(p.R1843M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23396794:23396794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2192C>T |
| AA Mutation | p.Ala731Val(p.A731V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384553:23384553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5454A>C |
| AA Mutation | p.Glu1818Asp(p.E1818D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23385035:23385035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5170A>G |
| AA Mutation | p.Ser1724Gly(p.S1724G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400759:23400759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1360C>T |
| AA Mutation | p.Arg454Cys(p.R454C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23407157:23407157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587782959 |
| CDS Mutation | c.67C>T |
| AA Mutation | p.Arg23Cys(p.R23C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384501:23384501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769228763 |
| CDS Mutation | c.5506G>A |
| AA Mutation | p.Ala1836Thr(p.A1836T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23386020:23386020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745747137 |
| CDS Mutation | c.5071C>T |
| AA Mutation | p.Arg1691Cys(p.R1691C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23387566:23387566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4613A>G |
| AA Mutation | p.Glu1538Gly(p.E1538G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23388952:23388952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533942127 |
| CDS Mutation | c.4082G>A |
| AA Mutation | p.Arg1361His(p.R1361H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384660:23384660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758734120 |
| CDS Mutation | c.5347C>T |
| AA Mutation | p.Arg1783Cys(p.R1783C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356287 |
| Start | 23393024:23393024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755565288 |
| CDS Mutation | c.3139C>T |
| AA Mutation | p.Arg1047Cys(p.R1047C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23390213:23390213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762573185 |
| CDS Mutation | c.3576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23394161:23394161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752148935 |
| CDS Mutation | c.2592G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23402766:23402766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371728824 |
| CDS Mutation | c.933C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23387888:23387888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74039310 |
| CDS Mutation | c.4395G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400721:23400721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745448722 |
| CDS Mutation | c.1398C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400868:23400868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543839082 |
| CDS Mutation | c.1251C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23392932:23392932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23404729:23404729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23397022:23397022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2109C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23404320:23404320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23405648:23405648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.324C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23403391:23403391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23384601:23384601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23393753:23393753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140305424 |
| CDS Mutation | c.2841C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23405117:23405117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.513C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23400388:23400388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145447555 |
| CDS Mutation | c.1449C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356287 |
| Start | 23402772:23402772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748779752 |
| CDS Mutation | c.927C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |