Primary Site >> Stomach Cancer
Gene >> ATG9A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219222150:219222150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2045C>G |
| AA Mutation | p.Ala682Gly(p.A682G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361242 |
| Start | 219226933:219226933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761159469 |
| CDS Mutation | c.148G>A |
| AA Mutation | p.Val50Ile(p.V50I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219225442:219225442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766008146 |
| CDS Mutation | c.343G>A |
| AA Mutation | p.Ala115Thr(p.A115T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219223912:219223912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1376C>T |
| AA Mutation | p.Ser459Leu(p.S459L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219222353:219222353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1946C>T |
| AA Mutation | p.Ala649Val(p.A649V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219224685:219224685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.686C>A |
| AA Mutation | p.Pro229His(p.P229H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219221143:219221143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2305C>G |
| AA Mutation | p.Pro769Ala(p.P769A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219224421:219224421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950C>T |
| AA Mutation | p.Ala317Val(p.A317V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219220794:219220794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2467G>A |
| AA Mutation | p.Val823Met(p.V823M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219223940:219223940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Asp450Asn(p.D450N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361242 |
| Start | 219222685:219222685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1808C>T |
| AA Mutation | p.Ala603Val(p.A603V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361242 |
| Start | 219224834:219224834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373511038 |
| CDS Mutation | c.537G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361242 |
| Start | 219225527:219225527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541694613 |
| CDS Mutation | c.258C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361242 |
| Start | 219222688:219222688(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1805delA |
| AA Mutation | p.Asn602MetfsTer17(p.N602Mfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000361242 |
| Start | 219224105:219224105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1265+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |