Primary Site >> Stomach Cancer
Gene >> SLC14A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45627083:45627083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457A>G |
| AA Mutation | p.Thr153Ala(p.T153A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45668359:45668359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758687472 |
| CDS Mutation | c.1918G>A |
| AA Mutation | p.Ala640Thr(p.A640T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45625758:45625758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758035710 |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Asp76Asn(p.D76N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45668470:45668470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2029A>G |
| AA Mutation | p.Met677Val(p.M677V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45624768:45624768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763235524 |
| CDS Mutation | c.104C>T |
| AA Mutation | p.Pro35Leu(p.P35L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45639821:45639821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919G>A |
| AA Mutation | p.Val307Met(p.V307M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45627047:45627047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421A>G |
| AA Mutation | p.Ile141Val(p.I141V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45682442:45682442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201444739 |
| CDS Mutation | c.2686C>T |
| AA Mutation | p.Arg896Cys(p.R896C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45637177:45637177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764757845 |
| CDS Mutation | c.838C>T |
| AA Mutation | p.Pro280Ser(p.P280S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45672939:45672939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142459777 |
| CDS Mutation | c.2269G>A |
| AA Mutation | p.Gly757Ser(p.G757S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45624749:45624749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.85A>G |
| AA Mutation | p.Ser29Gly(p.S29G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45637160:45637160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.821G>T |
| AA Mutation | p.Trp274Leu(p.W274L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255226 |
| Start | 45673748:45673748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755301577 |
| CDS Mutation | c.2443G>A |
| AA Mutation | p.Ala815Thr(p.A815T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45637002:45637002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.663T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45624769:45624769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115615745 |
| CDS Mutation | c.105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45625757:45625757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752273819 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45682384:45682384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556254338 |
| CDS Mutation | c.2628C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45682411:45682411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143610580 |
| CDS Mutation | c.2655G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45644135:45644135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201995847 |
| CDS Mutation | c.1326C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255226 |
| Start | 45682330:45682330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567587864 |
| CDS Mutation | c.2574G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000255226 |
| Start | 45673790:45673790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151319242 |
| CDS Mutation | c.2485C>T |
| AA Mutation | p.Gln829Ter(p.Q829*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |