Primary Site >> Stomach Cancer
Gene >> DCTN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74369410:74369410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1474G>T |
| AA Mutation | p.Ala492Ser(p.A492S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74363033:74363033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3490A>T |
| AA Mutation | p.Thr1164Ser(p.T1164S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74369347:74369347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1537T>C |
| AA Mutation | p.Tyr513His(p.Y513H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74366849:74366849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2400G>T |
| AA Mutation | p.Lys800Asn(p.K800N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74369423:74369423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1461G>T |
| AA Mutation | p.Glu487Asp(p.E487D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74365629:74365629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2915G>A |
| AA Mutation | p.Arg972Gln(p.R972Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74369356:74369356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1528G>A |
| AA Mutation | p.Val510Ile(p.V510I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74369993:74369993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763277715 |
| CDS Mutation | c.1364G>A |
| AA Mutation | p.Arg455His(p.R455H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74366579:74366579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2508G>T |
| AA Mutation | p.Trp836Cys(p.W836C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74370487:74370487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765995146 |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Arg369His(p.R369H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361874 |
| Start | 74371110:74371110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712C>T |
| AA Mutation | p.Arg238Trp(p.R238W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361874 |
| Start | 74362665:74362665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115689748 |
| CDS Mutation | c.3594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361874 |
| Start | 74370811:74370811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151107870 |
| CDS Mutation | c.858G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361874 |
| Start | 74370312:74370312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72659373 |
| CDS Mutation | c.1161G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |