Primary Site >> Stomach Cancer
Gene >> SFTPB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393822 |
| Start | 85665773:85665773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415C>T |
| AA Mutation | p.His139Tyr(p.H139Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393822 |
| Start | 85663464:85663464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780787602 |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Arg295Gln(p.R295Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393822 |
| Start | 85667776:85667776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.98C>G |
| AA Mutation | p.Ala33Gly(p.A33G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393822 |
| Start | 85663467:85663467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Pro294Leu(p.P294L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393822 |
| Start | 85665756:85665756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.432A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393822 |
| Start | 85665370:85665370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45530632 |
| CDS Mutation | c.591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |