Primary Site >> Stomach Cancer
Gene >> IFT172
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461345:27461345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148237432 |
| CDS Mutation | c.2366G>A |
| AA Mutation | p.Arg789Gln(p.R789Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27484235:27484235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.328A>G |
| AA Mutation | p.Ile110Val(p.I110V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27481065:27481065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777914345 |
| CDS Mutation | c.766G>A |
| AA Mutation | p.Val256Met(p.V256M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461815:27461815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2137G>A |
| AA Mutation | p.Gly713Ser(p.G713S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27477581:27477581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1199A>G |
| AA Mutation | p.Lys400Arg(p.K400R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461457:27461457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2254C>A |
| AA Mutation | p.Gln752Lys(p.Q752K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27459780:27459780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2571G>T |
| AA Mutation | p.Glu857Asp(p.E857D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27465486:27465486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1862C>T |
| AA Mutation | p.Thr621Ile(p.T621I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27457929:27457929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372047259 |
| CDS Mutation | c.3023A>G |
| AA Mutation | p.Lys1008Arg(p.K1008R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27472315:27472315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143520040 |
| CDS Mutation | c.1459C>T |
| AA Mutation | p.Arg487Cys(p.R487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27450059:27450059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202236985 |
| CDS Mutation | c.3989G>A |
| AA Mutation | p.Arg1330His(p.R1330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461341:27461341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2370G>T |
| AA Mutation | p.Glu790Asp(p.E790D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27447546:27447546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571220836 |
| CDS Mutation | c.4628C>T |
| AA Mutation | p.Thr1543Met(p.T1543M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27454587:27454587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3445G>T |
| AA Mutation | p.Ala1149Ser(p.A1149S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27465786:27465786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1789A>G |
| AA Mutation | p.Ile597Val(p.I597V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461027:27461027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752494593 |
| CDS Mutation | c.2509G>A |
| AA Mutation | p.Ala837Thr(p.A837T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27458184:27458184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2917C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27456525:27456525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76787560 |
| CDS Mutation | c.3357C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27465784:27465784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747273253 |
| CDS Mutation | c.1791C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27481075:27481075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.756C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461461:27461461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2250A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260570 |
| Start | 27461043:27461043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2493C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260570 |
| Start | 27481076:27481076(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.755delG |
| AA Mutation | p.Gly252AlafsTer6(p.G252Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260570 |
| Start | 27454065:27454065(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3628delG |
| AA Mutation | p.Ala1210ProfsTer107(p.A1210Pfs*107) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260570 |
| Start | 27459767:27459767(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2584delG |
| AA Mutation | p.Asp862ThrfsTer42(p.D862Tfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260570 |
| Start | 27459815:27459815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761095604 |
| CDS Mutation | c.2536C>T |
| AA Mutation | p.Arg846Ter(p.R846*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |