Primary Site >> Stomach Cancer
Gene >> ALK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29227661:29227661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2827G>A |
| AA Mutation | p.Ala943Thr(p.A943T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29532020:29532020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759426382 |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Ser350Leu(p.S350L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193396:29193396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4691C>T |
| AA Mutation | p.Ala1564Val(p.A1564V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29320825:29320825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1472A>C |
| AA Mutation | p.Gln491Pro(p.Q491P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193894:29193894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531490912 |
| CDS Mutation | c.4193C>T |
| AA Mutation | p.Pro1398Leu(p.P1398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29233692:29233692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2360A>G |
| AA Mutation | p.Asn787Ser(p.N787S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29920253:29920253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745712273 |
| CDS Mutation | c.407G>A |
| AA Mutation | p.Arg136Gln(p.R136Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193652:29193652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4435G>A |
| AA Mutation | p.Ala1479Thr(p.A1479T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29532080:29532080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781677582 |
| CDS Mutation | c.989A>G |
| AA Mutation | p.Lys330Arg(p.K330R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29920043:29920043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.617C>T |
| AA Mutation | p.Ala206Val(p.A206V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193676:29193676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201759867 |
| CDS Mutation | c.4411G>A |
| AA Mutation | p.Val1471Met(p.V1471M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29239774:29239774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2261C>T |
| AA Mutation | p.Ser754Phe(p.S754F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29532042:29532042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1027G>C |
| AA Mutation | p.Glu343Gln(p.E343Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29275221:29275221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1919G>A |
| AA Mutation | p.Gly640Glu(p.G640E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29694962:29694962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193287:29193287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4800A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29239767:29239767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149853746 |
| CDS Mutation | c.2268C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29251116:29251116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56017149 |
| CDS Mutation | c.2193C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193893:29193893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201653228 |
| CDS Mutation | c.4194G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193275:29193275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753750497 |
| CDS Mutation | c.4812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29920147:29920147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534035801 |
| CDS Mutation | c.513C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29227644:29227644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759086883 |
| CDS Mutation | c.2844C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29239806:29239806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111253753 |
| CDS Mutation | c.2229C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389048 |
| Start | 29223491:29223491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138178848 |
| CDS Mutation | c.3210G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389048 |
| Start | 29275147:29275147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1993A>T |
| AA Mutation | p.Lys665Ter(p.K665*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389048 |
| Start | 29232423:29232424(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2512dupC |
| AA Mutation | p.Leu838ProfsTer27(p.L838Pfs*27) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000389048 |
| Start | 29328349:29328349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777414641 |
| CDS Mutation | c.1414+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |