Primary Site >> Stomach Cancer
Gene >> CLDN10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376873 |
| Start | 95433997:95433997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Ala55Val(p.A55V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299339 |
| Start | 95552862:95552862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Gly37Ser(p.G37S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299339 |
| Start | 95552803:95552803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.50G>T |
| AA Mutation | p.Gly17Val(p.G17V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376873 |
| Start | 95434022:95434022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.189G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299339 |
| Start | 95560229:95560229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374567220 |
| CDS Mutation | c.318C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299339 |
| Start | 95577915:95577915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299339 |
| Start | 95577318:95577318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.552T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376873 |
| Start | 95433995:95433995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555827487 |
| CDS Mutation | c.162C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |