Primary Site >> Stomach Cancer
Gene >> PROX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997665:213997665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997563:213997563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763076142 |
| CDS Mutation | c.1028C>T |
| AA Mutation | p.Pro343Leu(p.P343L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213996552:213996552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.17G>A |
| AA Mutation | p.Ser6Asn(p.S6N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997061:213997061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.526A>G |
| AA Mutation | p.Met176Val(p.M176V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213996560:213996560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.25C>A |
| AA Mutation | p.Leu9Ile(p.L9I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213998250:213998250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1715C>T |
| AA Mutation | p.Ser572Leu(p.S572L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997012:213997012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.477T>A |
| AA Mutation | p.Asp159Glu(p.D159E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213996984:213996984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.449G>T |
| AA Mutation | p.Ser150Ile(p.S150I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997242:213997242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Arg236His(p.R236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997400:213997400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.865C>G |
| AA Mutation | p.Gln289Glu(p.Q289E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997679:213997679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777612764 |
| CDS Mutation | c.1144G>A |
| AA Mutation | p.Val382Ile(p.V382I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213998174:213998174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Ala547Thr(p.A547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997286:213997286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Arg251Cys(p.R251C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997052:213997052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517A>T |
| AA Mutation | p.Ile173Phe(p.I173F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997651:213997651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1116G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997333:213997333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.798G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997966:213997966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1431G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997411:213997411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779626865 |
| CDS Mutation | c.876C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |