Primary Site >> Stomach Cancer
Gene >> CADM3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193957:159193957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.608A>G |
| AA Mutation | p.Asp203Gly(p.D203G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193908:159193908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.559A>C |
| AA Mutation | p.Thr187Pro(p.T187P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193428:159193428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.388C>T |
| AA Mutation | p.Pro130Ser(p.P130S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193881:159193881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532C>T |
| AA Mutation | p.Arg178Cys(p.R178C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159199861:159199861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1063T>G |
| AA Mutation | p.Leu355Val(p.L355V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159192622:159192622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274G>A |
| AA Mutation | p.Glu92Lys(p.E92K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193492:159193492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452A>G |
| AA Mutation | p.Asn151Ser(p.N151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159196432:159196432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.760T>G |
| AA Mutation | p.Cys254Gly(p.C254G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159196376:159196376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778876352 |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Ala235Val(p.A235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159192718:159192718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.370G>A |
| AA Mutation | p.Val124Ile(p.V124I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159193917:159193917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568G>A |
| AA Mutation | p.Val190Ile(p.V190I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368125 |
| Start | 159191993:159191993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.146A>C |
| AA Mutation | p.Lys49Thr(p.K49T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368125 |
| Start | 159200898:159200898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569300786 |
| CDS Mutation | c.1173C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |