Primary Site >> Stomach Cancer
Gene >> COL17A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104035277:104035277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758851971 |
| CDS Mutation | c.3605C>T |
| AA Mutation | p.Ser1202Leu(p.S1202L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104050095:104050095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2158C>A |
| AA Mutation | p.Leu720Ile(p.L720I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104064524:104064524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568269377 |
| CDS Mutation | c.680C>T |
| AA Mutation | p.Ala227Val(p.A227V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104058179:104058179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1234A>T |
| AA Mutation | p.Thr412Ser(p.T412S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104053075:104053075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533717233 |
| CDS Mutation | c.1895G>A |
| AA Mutation | p.Arg632His(p.R632H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104047798:104047798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2276T>A |
| AA Mutation | p.Leu759His(p.L759H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104055976:104055976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371044491 |
| CDS Mutation | c.1493G>A |
| AA Mutation | p.Arg498His(p.R498H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104076322:104076322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766539630 |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Val104Ile(p.V104I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104049427:104049427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764552135 |
| CDS Mutation | c.2209G>A |
| AA Mutation | p.Gly737Arg(p.G737R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104032682:104032682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4430G>T |
| AA Mutation | p.Gly1477Val(p.G1477V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104063756:104063756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.829T>C |
| AA Mutation | p.Ser277Pro(p.S277P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104041311:104041311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2639G>A |
| AA Mutation | p.Gly880Asp(p.G880D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000353479 |
| Start | 104063813:104063813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139445116 |
| CDS Mutation | c.772G>A |
| AA Mutation | p.Gly258Arg(p.G258R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104070523:104070523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762634230 |
| CDS Mutation | c.510G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104035529:104035529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371031867 |
| CDS Mutation | c.3453G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104034748:104034748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104055978:104055978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143263539 |
| CDS Mutation | c.1491G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104063787:104063787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.798C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104038428:104038428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3048G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104038497:104038497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2979C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104037733:104037733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3111C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000353479 |
| Start | 104060180:104060180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1080G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000353479 |
| Start | 104059690:104059690(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769586532 |
| CDS Mutation | c.1170delA |
| AA Mutation | p.Glu391LysfsTer12(p.E391Kfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000353479 |
| Start | 104033944:104033944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373469159 |
| CDS Mutation | c.4156+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |