Primary Site >> Stomach Cancer
Gene >> EPHA7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93259473:93259473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1805T>A |
| AA Mutation | p.Phe602Tyr(p.F602Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93259476:93259476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1802A>C |
| AA Mutation | p.Lys601Thr(p.K601T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93358395:93358395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.849C>G |
| AA Mutation | p.Phe283Leu(p.F283L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93410977:93410977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.356G>T |
| AA Mutation | p.Cys119Phe(p.C119F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93410629:93410629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.704T>C |
| AA Mutation | p.Val235Ala(p.V235A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93410560:93410560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.773T>G |
| AA Mutation | p.Val258Gly(p.V258G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93258177:93258177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2032G>A |
| AA Mutation | p.Asp678Asn(p.D678N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93246963:93246963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2555G>A |
| AA Mutation | p.Gly852Asp(p.G852D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369303 |
| Start | 93257464:93257464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2170A>G |
| AA Mutation | p.Arg724Gly(p.R724G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93269536:93269536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1574A>C |
| AA Mutation | p.Asn525Thr(p.N525T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93245390:93245390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2790A>T |
| AA Mutation | p.Glu930Asp(p.E930D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93356953:93356953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1088T>C |
| AA Mutation | p.Val363Ala(p.V363A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93246957:93246957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776802108 |
| CDS Mutation | c.2561G>A |
| AA Mutation | p.Arg854His(p.R854H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93269537:93269537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569672013 |
| CDS Mutation | c.1573A>C |
| AA Mutation | p.Asn525His(p.N525H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93358376:93358376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868G>T |
| AA Mutation | p.Asp290Tyr(p.D290Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369303 |
| Start | 93255853:93255853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2357A>C |
| AA Mutation | p.Asp786Ala(p.D786A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369303 |
| Start | 93411039:93411039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.294T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369303 |
| Start | 93272304:93272304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769720060 |
| CDS Mutation | c.1443C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000369303 |
| Start | 93272296:93272296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1449+2T>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |