Primary Site >> Stomach Cancer
Gene >> DAAM2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39873253:39873253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060A>C |
| AA Mutation | p.Lys354Gln(p.K354Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39888704:39888704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773938955 |
| CDS Mutation | c.2086C>T |
| AA Mutation | p.Arg696Trp(p.R696W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39860976:39860976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217C>T |
| AA Mutation | p.Pro73Ser(p.P73S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39888732:39888732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2114A>T |
| AA Mutation | p.Gln705Leu(p.Q705L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39896931:39896931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2461C>T |
| AA Mutation | p.Arg821Trp(p.R821W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39902011:39902011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747447552 |
| CDS Mutation | c.3181C>T |
| AA Mutation | p.Arg1061Trp(p.R1061W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39901963:39901963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772498031 |
| CDS Mutation | c.3133C>T |
| AA Mutation | p.Arg1045Cys(p.R1045C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39902023:39902023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775538347 |
| CDS Mutation | c.3193C>T |
| AA Mutation | p.Arg1065Trp(p.R1065W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39878255:39878255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762052729 |
| CDS Mutation | c.1354C>T |
| AA Mutation | p.Arg452Trp(p.R452W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39896892:39896892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2422T>G |
| AA Mutation | p.Phe808Val(p.F808V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39901976:39901976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200618513 |
| CDS Mutation | c.3146G>A |
| AA Mutation | p.Arg1049Gln(p.R1049Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39901453:39901453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750047168 |
| CDS Mutation | c.2963G>A |
| AA Mutation | p.Arg988Gln(p.R988Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39856306:39856306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4G>A |
| AA Mutation | p.Ala2Thr(p.A2T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274867 |
| Start | 39879346:39879346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1714C>A |
| AA Mutation | p.Pro572Thr(p.P572T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274867 |
| Start | 39867555:39867555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.474A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000274867 |
| Start | 39901975:39901975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759817118 |
| CDS Mutation | c.3145C>T |
| AA Mutation | p.Arg1049Ter(p.R1049*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |