Primary Site >> Stomach Cancer
Gene >> CNTN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205073146:205073146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2923G>A |
| AA Mutation | p.Glu975Lys(p.E975K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205072080:205072080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2678G>C |
| AA Mutation | p.Arg893Pro(p.R893P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205061981:205061981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1090G>A |
| AA Mutation | p.Gly364Arg(p.G364R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205070007:205070007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2377C>T |
| AA Mutation | p.Arg793Cys(p.R793C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205070025:205070025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766215909 |
| CDS Mutation | c.2395G>A |
| AA Mutation | p.Glu799Lys(p.E799K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205064388:205064388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1307T>A |
| AA Mutation | p.Ile436Asn(p.I436N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205061268:205061268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200893856 |
| CDS Mutation | c.821G>A |
| AA Mutation | p.Arg274His(p.R274H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205069550:205069550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773485559 |
| CDS Mutation | c.2185G>A |
| AA Mutation | p.Val729Ile(p.V729I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205065865:205065865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1772C>T |
| AA Mutation | p.Thr591Met(p.T591M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205065879:205065879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556646437 |
| CDS Mutation | c.1786G>A |
| AA Mutation | p.Ala596Thr(p.A596T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205062551:205062551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Ala408Thr(p.A408T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205069858:205069858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2228G>T |
| AA Mutation | p.Gly743Val(p.G743V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205064667:205064667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1436G>A |
| AA Mutation | p.Ser479Asn(p.S479N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331830 |
| Start | 205065821:205065821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766092588 |
| CDS Mutation | c.1728C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331830 |
| Start | 205071985:205071985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115143667 |
| CDS Mutation | c.2583G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |