Primary Site >> Stomach Cancer
Gene >> TTLL5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75902219:75902219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3818C>G |
| AA Mutation | p.Ser1273Cys(p.S1273C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75863791:75863791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377099575 |
| CDS Mutation | c.3451G>T |
| AA Mutation | p.Ala1151Ser(p.A1151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75776763:75776763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2300C>A |
| AA Mutation | p.Ala767Asp(p.A767D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75783335:75783335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2791C>G |
| AA Mutation | p.Gln931Glu(p.Q931E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75771816:75771816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2098T>C |
| AA Mutation | p.Phe700Leu(p.F700L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75863741:75863741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3401T>C |
| AA Mutation | p.Val1134Ala(p.V1134A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75771807:75771807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367910225 |
| CDS Mutation | c.2089G>A |
| AA Mutation | p.Gly697Ser(p.G697S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75779646:75779646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2459C>A |
| AA Mutation | p.Thr820Asn(p.T820N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75752940:75752940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770398766 |
| CDS Mutation | c.1535G>A |
| AA Mutation | p.Arg512His(p.R512H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75771762:75771762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044G>A |
| AA Mutation | p.Ala682Thr(p.A682T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75690278:75690278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.458T>C |
| AA Mutation | p.Leu153Pro(p.L153P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75683652:75683652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.367C>G |
| AA Mutation | p.Pro123Ala(p.P123A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75863854:75863854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763081813 |
| CDS Mutation | c.3514C>T |
| AA Mutation | p.Arg1172Trp(p.R1172W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75775557:75775557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762742540 |
| CDS Mutation | c.2210G>A |
| AA Mutation | p.Arg737Gln(p.R737Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75699247:75699247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773542134 |
| CDS Mutation | c.562C>T |
| AA Mutation | p.Arg188Trp(p.R188W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75669483:75669483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142G>A |
| AA Mutation | p.Ala48Thr(p.A48T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298832 |
| Start | 75669502:75669502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.161A>T |
| AA Mutation | p.Asn54Ile(p.N54I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75783508:75783508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2964T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75902154:75902154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142835737 |
| CDS Mutation | c.3753G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75902160:75902160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3759G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75783469:75783469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2925C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75783220:75783220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2676G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298832 |
| Start | 75669476:75669476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.135T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298832 |
| Start | 75690279:75690279(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.463delC |
| AA Mutation | p.Gln155ArgfsTer24(p.Q155Rfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000298832 |
| Start | 75775559:75775559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377702881 |
| CDS Mutation | c.2212C>T |
| AA Mutation | p.Arg738Ter(p.R738*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |