Primary Site >> Stomach Cancer
Gene >> CSF3R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36472663:36472663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150616658 |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Arg233Trp(p.R233W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36472653:36472653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707A>G |
| AA Mutation | p.Asp236Gly(p.D236G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36475383:36475383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142999683 |
| CDS Mutation | c.355G>A |
| AA Mutation | p.Ala119Thr(p.A119T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36466515:36466515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2353A>G |
| AA Mutation | p.Lys785Glu(p.K785E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36466751:36466751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2117C>A |
| AA Mutation | p.Pro706Gln(p.P706Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36471622:36471622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768170625 |
| CDS Mutation | c.1096G>A |
| AA Mutation | p.Gly366Arg(p.G366R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36473576:36473576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186379741 |
| CDS Mutation | c.532G>A |
| AA Mutation | p.Val178Met(p.V178M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36479438:36479438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.59C>T |
| AA Mutation | p.Pro20Leu(p.P20L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361632 |
| Start | 36472357:36472357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.878A>C |
| AA Mutation | p.Glu293Ala(p.E293A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361632 |
| Start | 36469223:36469223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142503546 |
| CDS Mutation | c.1509C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361632 |
| Start | 36472664:36472664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.696G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361632 |
| Start | 36469758:36469758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361632 |
| Start | 36475384:36475384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368386515 |
| CDS Mutation | c.354C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361632 |
| Start | 36469722:36469722(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769210858 |
| CDS Mutation | c.1404delC |
| AA Mutation | p.Ser469AlafsTer22(p.S469Afs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361632 |
| Start | 36469695:36469695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1431G>A |
| AA Mutation | p.Trp477Ter(p.W477*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361632 |
| Start | 36479465:36479466(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.31dupT |
| AA Mutation | p.Trp11LeufsTer70(p.W11Lfs*70) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |