Primary Site >> Stomach Cancer
Gene >> MFN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11992648:11992648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269A>G |
| AA Mutation | p.Glu90Gly(p.E90G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 12001483:12001483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899G>A |
| AA Mutation | p.Arg300His(p.R300H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11997390:11997390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.568C>A |
| AA Mutation | p.Leu190Ile(p.L190I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11999082:11999082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803A>C |
| AA Mutation | p.Glu268Ala(p.E268A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11999055:11999055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755065651 |
| CDS Mutation | c.776G>A |
| AA Mutation | p.Arg259His(p.R259H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 12009709:12009709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2187C>G |
| AA Mutation | p.Ser729Arg(p.S729R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11998796:11998796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.626T>C |
| AA Mutation | p.Leu209Pro(p.L209P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11997337:11997337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515A>G |
| AA Mutation | p.Gln172Arg(p.Q172R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 12005906:12005906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746213217 |
| CDS Mutation | c.1691G>A |
| AA Mutation | p.Arg564Gln(p.R564Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235329 |
| Start | 11992687:11992687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308G>T |
| AA Mutation | p.Gly103Val(p.G103V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235329 |
| Start | 12001773:12001773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141475476 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235329 |
| Start | 12007115:12007115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752881611 |
| CDS Mutation | c.1935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |