Primary Site >> Stomach Cancer
Gene >> CADM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115229220:115229220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.614T>G |
| AA Mutation | p.Leu205Arg(p.L205R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115231481:115231481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768807528 |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Arg145His(p.R145H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115231426:115231426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489A>C |
| AA Mutation | p.Glu163Asp(p.E163D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000452722 |
| Start | 115240274:115240274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.271C>T |
| AA Mutation | p.Pro91Ser(p.P91S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115217928:115217928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785C>T |
| AA Mutation | p.Ala262Val(p.A262V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115214667:115214667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935G>A |
| AA Mutation | p.Arg312His(p.R312H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115231413:115231413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Ala168Thr(p.A168T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115217932:115217932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.781G>A |
| AA Mutation | p.Asp261Asn(p.D261N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115178767:115178767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1087G>T |
| AA Mutation | p.Ala363Ser(p.A363S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115178689:115178689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1165C>A |
| AA Mutation | p.Leu389Met(p.L389M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115217944:115217944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769A>C |
| AA Mutation | p.Thr257Pro(p.T257P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115229119:115229119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715G>T |
| AA Mutation | p.Val239Leu(p.V239L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115231434:115231434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.481G>A |
| AA Mutation | p.Glu161Lys(p.E161K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000452722 |
| Start | 115240418:115240418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.127G>A |
| AA Mutation | p.Asp43Asn(p.D43N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115209654:115209654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998C>A |
| AA Mutation | p.Pro333His(p.P333H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000452722 |
| Start | 115176545:115176545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1258G>A |
| AA Mutation | p.Ala420Thr(p.A420T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000452722 |
| Start | 115214729:115214729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528617309 |
| CDS Mutation | c.873C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |