Primary Site >> Stomach Cancer
Gene >> EXTL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28716093:28716093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Ala12Thr(p.A12T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28750826:28750826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2720G>A |
| AA Mutation | p.Arg907His(p.R907H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28716148:28716148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.89C>T |
| AA Mutation | p.Thr30Met(p.T30M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717900:28717900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1841T>C |
| AA Mutation | p.Phe614Ser(p.F614S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28718196:28718196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774554716 |
| CDS Mutation | c.2137G>A |
| AA Mutation | p.Val713Ile(p.V713I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717725:28717725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755902308 |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Arg556Cys(p.R556C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717069:28717069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1010T>C |
| AA Mutation | p.Val337Ala(p.V337A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717669:28717669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769181445 |
| CDS Mutation | c.1610G>A |
| AA Mutation | p.Arg537His(p.R537H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717326:28717326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1267G>A |
| AA Mutation | p.Glu423Lys(p.E423K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28737571:28737571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2329G>A |
| AA Mutation | p.Ala777Thr(p.A777T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717486:28717486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1427T>C |
| AA Mutation | p.Leu476Pro(p.L476P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28750663:28750663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2557T>G |
| AA Mutation | p.Ser853Ala(p.S853A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28716963:28716963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.904A>G |
| AA Mutation | p.Thr302Ala(p.T302A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28716766:28716766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Cys236Tyr(p.C236Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28731323:28731323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2249G>A |
| AA Mutation | p.Arg750His(p.R750H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220562 |
| Start | 28743168:28743168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2504C>T |
| AA Mutation | p.Ala835Val(p.A835V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220562 |
| Start | 28743142:28743142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2478T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717685:28717685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140625555 |
| CDS Mutation | c.1626C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717514:28717514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1455G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717322:28717322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1263C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220562 |
| Start | 28716644:28716644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754413534 |
| CDS Mutation | c.585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220562 |
| Start | 28717363:28717363(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1308delC |
| AA Mutation | p.Asp438ThrfsTer71(p.D438Tfs*71) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |