Primary Site >> Stomach Cancer
Gene >> TLR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704267:153704267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766467979 |
| CDS Mutation | c.1360T>C |
| AA Mutation | p.Cys454Arg(p.C454R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260010 |
| Start | 153702956:153702956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.49C>A |
| AA Mutation | p.Leu17Ile(p.L17I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260010 |
| Start | 153705212:153705212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772688052 |
| CDS Mutation | c.2305G>T |
| AA Mutation | p.Ala769Ser(p.A769S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704856:153704856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200483398 |
| CDS Mutation | c.1949G>A |
| AA Mutation | p.Arg650Gln(p.R650Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704337:153704337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745540048 |
| CDS Mutation | c.1430C>T |
| AA Mutation | p.Pro477Leu(p.P477L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153703841:153703841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.934T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704338:153704338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150700268 |
| CDS Mutation | c.1431G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153703471:153703471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704578:153704578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751237112 |
| CDS Mutation | c.1671T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153703249:153703249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.342T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260010 |
| Start | 153704623:153704623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772226208 |
| CDS Mutation | c.1716C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260010 |
| Start | 153704339:153704339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1432C>T |
| AA Mutation | p.Gln478Ter(p.Q478*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |