Primary Site >> Stomach Cancer
Gene >> EHMT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31884464:31884464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760598456 |
| CDS Mutation | c.2699C>T |
| AA Mutation | p.Ala900Val(p.A900V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31882948:31882948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3056A>G |
| AA Mutation | p.Gln1019Arg(p.Q1019R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31880721:31880721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3404G>A |
| AA Mutation | p.Arg1135His(p.R1135H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31889302:31889302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201104297 |
| CDS Mutation | c.1040G>A |
| AA Mutation | p.Arg347Gln(p.R347Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31884446:31884446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2717A>T |
| AA Mutation | p.Lys906Met(p.K906M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31880691:31880691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760598540 |
| CDS Mutation | c.3434G>A |
| AA Mutation | p.Arg1145Gln(p.R1145Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31882768:31882768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3128A>G |
| AA Mutation | p.Tyr1043Cys(p.Y1043C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31887821:31887821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1886G>A |
| AA Mutation | p.Arg629Gln(p.R629Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31883867:31883867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2855A>G |
| AA Mutation | p.Tyr952Cys(p.Y952C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375537 |
| Start | 31884413:31884413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2750G>A |
| AA Mutation | p.Arg917His(p.R917H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31887811:31887811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1896G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31888680:31888680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31896619:31896619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31889057:31889057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31887587:31887587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375537 |
| Start | 31887052:31887052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762523692 |
| CDS Mutation | c.2061G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375537 |
| Start | 31884685:31884685(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2563delC |
| AA Mutation | p.Leu855CysfsTer36(p.L855Cfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375537 |
| Start | 31896986:31896986(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.46delG |
| AA Mutation | p.Glu16ArgfsTer68(p.E16Rfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375537 |
| Start | 31889303:31889303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756538741 |
| CDS Mutation | c.1039C>T |
| AA Mutation | p.Arg347Ter(p.R347*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000375537 |
| Start | 31884911:31884911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757379655 |
| CDS Mutation | c.2448+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000375537 |
| Start | 31889496:31889507(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs756298483 |
| CDS Mutation | c.960_971delAGAAGAGGAAGA |
| AA Mutation | p.Glu320_Glu323del(p.E320_E323del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |