Primary Site >> Stomach Cancer
Gene >> HDAC7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47789569:47789569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1984G>A |
| AA Mutation | p.Ala662Thr(p.A662T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47789560:47789560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1993C>T |
| AA Mutation | p.Arg665Trp(p.R665W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47791926:47791926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777217285 |
| CDS Mutation | c.1640G>A |
| AA Mutation | p.Arg547His(p.R547H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47785435:47785435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750793586 |
| CDS Mutation | c.2626C>T |
| AA Mutation | p.Pro876Ser(p.P876S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47796211:47796211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771710279 |
| CDS Mutation | c.674C>T |
| AA Mutation | p.Ser225Leu(p.S225L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47797488:47797488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.356C>T |
| AA Mutation | p.Pro119Leu(p.P119L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47795221:47795221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757098292 |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47789287:47789287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766456680 |
| CDS Mutation | c.2092G>A |
| AA Mutation | p.Ala698Thr(p.A698T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427332 |
| Start | 47794861:47794861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142887723 |
| CDS Mutation | c.1240G>A |
| AA Mutation | p.Gly414Arg(p.G414R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427332 |
| Start | 47791656:47791656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1746T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427332 |
| Start | 47798635:47798635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.159G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427332 |
| Start | 47798155:47798155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762278141 |
| CDS Mutation | c.297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427332 |
| Start | 47794862:47794862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1239C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000427332 |
| Start | 47787744:47787744(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2304delC |
| AA Mutation | p.Met769TrpfsTer12(p.M769Wfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000427332 |
| Start | 47795261:47795262(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs750203996 |
| CDS Mutation | c.1089dupC |
| AA Mutation | p.Ser364GlnfsTer33(p.S364Qfs*33) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |