Primary Site >> Stomach Cancer
Gene >> SPATS2L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200477880:200477880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1526G>T |
| AA Mutation | p.Arg509Leu(p.R509L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200419385:200419385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754518191 |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Glu112Lys(p.E112K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200472973:200472973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1202A>C |
| AA Mutation | p.Lys401Thr(p.K401T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200472952:200472952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1181A>T |
| AA Mutation | p.His394Leu(p.H394L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200440699:200440699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703C>G |
| AA Mutation | p.Leu235Val(p.L235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200439301:200439301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625A>C |
| AA Mutation | p.Lys209Gln(p.K209Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200467388:200467388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.946G>A |
| AA Mutation | p.Ala316Thr(p.A316T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358677 |
| Start | 200469972:200469972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1016G>T |
| AA Mutation | p.Cys339Phe(p.C339F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358677 |
| Start | 200478019:200478019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369093749 |
| CDS Mutation | c.1665G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000358677 |
| Start | 200473052:200473053(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1281_1281+1insAATGGATCTTCTAACCAAAGACGGA |
| AA Mutation | p.Arg436LysfsTer5(p.R436Kfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |