Primary Site >> Stomach Cancer
Gene >> IL17RA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319363 |
| Start | 17109450:17109450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2231T>C |
| AA Mutation | p.Val744Ala(p.V744A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319363 |
| Start | 17108539:17108539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1320C>A |
| AA Mutation | p.Asn440Lys(p.N440K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319363 |
| Start | 17108378:17108378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1159G>A |
| AA Mutation | p.Asp387Asn(p.D387N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319363 |
| Start | 17100358:17100358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145378071 |
| CDS Mutation | c.427C>T |
| AA Mutation | p.Arg143Cys(p.R143C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319363 |
| Start | 17108732:17108732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761567739 |
| CDS Mutation | c.1513A>G |
| AA Mutation | p.Ser505Gly(p.S505G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17097918:17097918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17108551:17108551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1332C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17109520:17109520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2301C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17102164:17102164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200114306 |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17108392:17108392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761716238 |
| CDS Mutation | c.1173C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17098815:17098815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.351G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319363 |
| Start | 17109424:17109424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776615984 |
| CDS Mutation | c.2205G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |