Primary Site >> Stomach Cancer
Gene >> TNN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175118740:175118740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2566A>G |
| AA Mutation | p.Arg856Gly(p.R856G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079467:175079467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549305847 |
| CDS Mutation | c.544G>A |
| AA Mutation | p.Val182Met(p.V182M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175097467:175097467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568708471 |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Ala547Thr(p.A547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175128089:175128089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548328539 |
| CDS Mutation | c.3103G>A |
| AA Mutation | p.Ala1035Thr(p.A1035T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175098386:175098386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144603425 |
| CDS Mutation | c.1910C>T |
| AA Mutation | p.Thr637Met(p.T637M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175118705:175118705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2531G>T |
| AA Mutation | p.Gly844Val(p.G844V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175117113:175117113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201010782 |
| CDS Mutation | c.2294C>T |
| AA Mutation | p.Thr765Met(p.T765M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077819:175077819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401G>A |
| AA Mutation | p.Gly134Glu(p.G134E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175080199:175080199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778199951 |
| CDS Mutation | c.821C>T |
| AA Mutation | p.Thr274Met(p.T274M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175080226:175080226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.848A>C |
| AA Mutation | p.Glu283Ala(p.E283A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175080389:175080389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1011A>C |
| AA Mutation | p.Glu337Asp(p.E337D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175094106:175094106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1441G>T |
| AA Mutation | p.Asp481Tyr(p.D481Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175085414:175085414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244C>T |
| AA Mutation | p.Pro415Leu(p.P415L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175118680:175118680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758686482 |
| CDS Mutation | c.2506G>A |
| AA Mutation | p.Gly836Arg(p.G836R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175123504:175123504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2755T>C |
| AA Mutation | p.Tyr919His(p.Y919H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175097493:175097493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1665G>T |
| AA Mutation | p.Gln555His(p.Q555H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175126994:175126994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182894731 |
| CDS Mutation | c.2954C>T |
| AA Mutation | p.Thr985Met(p.T985M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077522:175077522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.104A>C |
| AA Mutation | p.Asn35Thr(p.N35T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077687:175077687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269T>A |
| AA Mutation | p.Ile90Asn(p.I90N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175127023:175127023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2983C>T |
| AA Mutation | p.Pro995Ser(p.P995S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175098500:175098500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2024T>C |
| AA Mutation | p.Leu675Pro(p.L675P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175097485:175097485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657C>A |
| AA Mutation | p.Pro553Thr(p.P553T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175098375:175098375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1899G>C |
| AA Mutation | p.Glu633Asp(p.E633D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175144539:175144539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3748A>G |
| AA Mutation | p.Lys1250Glu(p.K1250E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175098427:175098427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201064305 |
| CDS Mutation | c.1951G>A |
| AA Mutation | p.Val651Met(p.V651M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079560:175079560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637G>A |
| AA Mutation | p.Val213Met(p.V213M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175097487:175097487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147951218 |
| CDS Mutation | c.1659G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175098426:175098426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759866598 |
| CDS Mutation | c.1950C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079574:175079574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175123404:175123404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2655T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175080200:175080200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747275638 |
| CDS Mutation | c.822G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077562:175077562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147634808 |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077635:175077635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079661:175079661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175128626:175128626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3210C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175117060:175117060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377310021 |
| CDS Mutation | c.2241C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175077595:175077595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079421:175079421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239462 |
| Start | 175079445:175079445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374925420 |
| CDS Mutation | c.522G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000239462 |
| Start | 175118571:175118571(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2401delC |
| AA Mutation | p.Gln801LysfsTer8(p.Q801Kfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000239462 |
| Start | 175097415:175097415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1589-2A>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |