Primary Site >> Stomach Cancer
Gene >> NNT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43644750:43644750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1238A>G |
| AA Mutation | p.Asp413Gly(p.D413G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43659213:43659213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2497G>A |
| AA Mutation | p.Val833Ile(p.V833I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43653087:43653087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759786744 |
| CDS Mutation | c.1933C>T |
| AA Mutation | p.Arg645Cys(p.R645C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43613045:43613045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751169858 |
| CDS Mutation | c.289G>A |
| AA Mutation | p.Glu97Lys(p.E97K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43655894:43655894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2114C>T |
| AA Mutation | p.Ala705Val(p.A705V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43624041:43624041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761727766 |
| CDS Mutation | c.697G>A |
| AA Mutation | p.Val233Ile(p.V233I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43700139:43700139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2897C>A |
| AA Mutation | p.Ala966Glu(p.A966E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43653205:43653205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2051G>A |
| AA Mutation | p.Gly684Asp(p.G684D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43609301:43609301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106T>G |
| AA Mutation | p.Phe36Val(p.F36V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264663 |
| Start | 43619104:43619104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.672A>C |
| AA Mutation | p.Lys224Asn(p.K224N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43651827:43651827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200162492 |
| CDS Mutation | c.1806C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43609261:43609261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.66C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43609336:43609336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43656729:43656729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371081845 |
| CDS Mutation | c.2370C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43644263:43644263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264663 |
| Start | 43655913:43655913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373432420 |
| CDS Mutation | c.2133T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |