Primary Site >> Stomach Cancer
Gene >> KIF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39596178:39596178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.722T>C |
| AA Mutation | p.Val241Ala(p.V241A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39360428:39360428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2049A>C |
| AA Mutation | p.Glu683Asp(p.E683D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39336535:39336535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2442T>A |
| AA Mutation | p.Asn814Lys(p.N814K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39540183:39540183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1465G>T |
| AA Mutation | p.Ala489Ser(p.A489S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39545623:39545623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201860401 |
| CDS Mutation | c.1247C>T |
| AA Mutation | p.Ala416Val(p.A416V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39720730:39720730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.148A>G |
| AA Mutation | p.Asn50Asp(p.N50D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39431103:39431103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1704C>A |
| AA Mutation | p.Asp568Glu(p.D568E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39540026:39540026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1622C>T |
| AA Mutation | p.Ser541Phe(p.S541F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39613230:39613230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.598A>G |
| AA Mutation | p.Asn200Asp(p.N200D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287152 |
| Start | 39714744:39714744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.199G>T |
| AA Mutation | p.Asp67Tyr(p.D67Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39545622:39545622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748097675 |
| CDS Mutation | c.1248G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39725280:39725280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.31A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39540043:39540043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1605C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39343758:39343758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143657366 |
| CDS Mutation | c.2379G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39357324:39357324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2133G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39596189:39596189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.711A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287152 |
| Start | 39357348:39357348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763515741 |
| CDS Mutation | c.2109C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000287152 |
| Start | 39613217:39613217(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.611delT |
| AA Mutation | p.Leu204Ter(p.L204*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000287152 |
| Start | 39540081:39540081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145150015 |
| CDS Mutation | c.1567C>T |
| AA Mutation | p.Arg523Ter(p.R523*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |