Primary Site >> Stomach Cancer
Gene >> EPHB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100807513:100807513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773679415 |
| CDS Mutation | c.2186G>A |
| AA Mutation | p.Arg729Gln(p.R729Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100813666:100813666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1742A>G |
| AA Mutation | p.Tyr581Cys(p.Y581C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100812865:100812865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2000T>C |
| AA Mutation | p.Ile667Thr(p.I667T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100803472:100803472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2953C>A |
| AA Mutation | p.Pro985Thr(p.P985T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100805543:100805543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2636G>A |
| AA Mutation | p.Arg879Gln(p.R879Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100803474:100803474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2951C>A |
| AA Mutation | p.Ala984Asp(p.A984D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100805690:100805690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2489T>C |
| AA Mutation | p.Ile830Thr(p.I830T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100812767:100812767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2098G>A |
| AA Mutation | p.Ala700Thr(p.A700T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100805535:100805535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34918225 |
| CDS Mutation | c.2644G>A |
| AA Mutation | p.Ala882Thr(p.A882T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100812896:100812896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1969C>G |
| AA Mutation | p.Gln657Glu(p.Q657E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100820204:100820204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749289689 |
| CDS Mutation | c.901G>A |
| AA Mutation | p.Val301Ile(p.V301I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100819596:100819596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61735975 |
| CDS Mutation | c.1258G>A |
| AA Mutation | p.Val420Ile(p.V420I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100822508:100822508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571C>T |
| AA Mutation | p.His191Tyr(p.H191Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100805656:100805656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775373372 |
| CDS Mutation | c.2523G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100819771:100819771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775159333 |
| CDS Mutation | c.1083C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100806486:100806486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377702127 |
| CDS Mutation | c.2418C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100819759:100819759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1095A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100817300:100817300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100823788:100823788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150582750 |
| CDS Mutation | c.267G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |