Primary Site >> Stomach Cancer
Gene >> PTPN14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214369606:214369606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3122C>G |
| AA Mutation | p.Thr1041Ser(p.T1041S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214378064:214378064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2583G>T |
| AA Mutation | p.Gln861His(p.Q861H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384108:214384108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1747G>A |
| AA Mutation | p.Ala583Thr(p.A583T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384546:214384546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1309C>T |
| AA Mutation | p.Pro437Ser(p.P437S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384126:214384126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1729A>G |
| AA Mutation | p.Thr577Ala(p.T577A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384693:214384693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190693661 |
| CDS Mutation | c.1162G>A |
| AA Mutation | p.Val388Met(p.V388M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384191:214384191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776055399 |
| CDS Mutation | c.1664C>T |
| AA Mutation | p.Thr555Met(p.T555M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214464665:214464665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.139C>A |
| AA Mutation | p.Leu47Met(p.L47M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214414676:214414676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139895368 |
| CDS Mutation | c.395G>A |
| AA Mutation | p.Arg132Gln(p.R132Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214364636:214364636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767244490 |
| CDS Mutation | c.3311A>G |
| AA Mutation | p.Asn1104Ser(p.N1104S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214383442:214383442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146980027 |
| CDS Mutation | c.2413G>A |
| AA Mutation | p.Gly805Ser(p.G805S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214401733:214401733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199664215 |
| CDS Mutation | c.621T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214464678:214464678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.126A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384001:214384001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1854T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214464696:214464696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748318666 |
| CDS Mutation | c.108G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384247:214384247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369464407 |
| CDS Mutation | c.1608G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214383884:214383884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761909201 |
| CDS Mutation | c.1971G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |