Primary Site >> Stomach Cancer
Gene >> GALNT6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51365519:51365519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.725G>A |
| AA Mutation | p.Arg242Gln(p.R242Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51359212:51359212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780755779 |
| CDS Mutation | c.1288C>T |
| AA Mutation | p.Arg430Cys(p.R430C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51365508:51365508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145549042 |
| CDS Mutation | c.736C>T |
| AA Mutation | p.Arg246Trp(p.R246W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51357399:51357399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142431103 |
| CDS Mutation | c.1552G>A |
| AA Mutation | p.Gly518Arg(p.G518R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51359287:51359287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373677203 |
| CDS Mutation | c.1213G>A |
| AA Mutation | p.Val405Ile(p.V405I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51379300:51379300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751562757 |
| CDS Mutation | c.482G>A |
| AA Mutation | p.Arg161Gln(p.R161Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356317 |
| Start | 51364146:51364146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777730506 |
| CDS Mutation | c.1024C>T |
| AA Mutation | p.Arg342Cys(p.R342C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356317 |
| Start | 51355827:51355827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139828720 |
| CDS Mutation | c.1734C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356317 |
| Start | 51377335:51377335(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.524delC |
| AA Mutation | p.Pro175HisfsTer7(p.P175Hfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356317 |
| Start | 51379563:51379564(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.218_219insAATGTTAG |
| AA Mutation | p.Arg74MetfsTer15(p.R74Mfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |