Primary Site >> Stomach Cancer
Gene >> DAAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59323011:59323011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560C>T |
| AA Mutation | p.Ala187Val(p.A187V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59323118:59323118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759856885 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Val223Met(p.V223M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59331840:59331840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139553997 |
| CDS Mutation | c.1888G>A |
| AA Mutation | p.Glu630Lys(p.E630K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59367576:59367576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773103520 |
| CDS Mutation | c.3004C>T |
| AA Mutation | p.Arg1002Cys(p.R1002C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59263559:59263559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.82T>C |
| AA Mutation | p.Tyr28His(p.Y28H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59324162:59324162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754289580 |
| CDS Mutation | c.809G>A |
| AA Mutation | p.Arg270Gln(p.R270Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59352603:59352603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2268G>T |
| AA Mutation | p.Lys756Asn(p.K756N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59352573:59352573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2238A>T |
| AA Mutation | p.Glu746Asp(p.E746D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000395125 |
| Start | 59331210:59331210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1562G>C |
| AA Mutation | p.Arg521Thr(p.R521T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59324375:59324375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910C>A |
| AA Mutation | p.Leu304Ile(p.L304I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59326634:59326634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1299G>C |
| AA Mutation | p.Lys433Asn(p.K433N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59340101:59340101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2026C>A |
| AA Mutation | p.Leu676Met(p.L676M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59324387:59324387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922T>A |
| AA Mutation | p.Phe308Ile(p.F308I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59368675:59368675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753779506 |
| CDS Mutation | c.3053G>A |
| AA Mutation | p.Arg1018His(p.R1018H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59355228:59355228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2450T>C |
| AA Mutation | p.Val817Ala(p.V817A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395125 |
| Start | 59347566:59347566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2133A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395125 |
| Start | 59326975:59326975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747424195 |
| CDS Mutation | c.1356G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000395125 |
| Start | 59359476:59359476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148831209 |
| CDS Mutation | c.2635C>T |
| AA Mutation | p.Arg879Ter(p.R879*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |