Primary Site >> Stomach Cancer
Gene >> NTRK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84955318:84955318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1925G>A |
| AA Mutation | p.Gly642Asp(p.G642D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84727872:84727872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1072G>T |
| AA Mutation | p.Asp358Tyr(p.D358Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84670942:84670942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.194C>A |
| AA Mutation | p.Pro65His(p.P65H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84724306:84724306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803C>T |
| AA Mutation | p.Ala268Val(p.A268V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 85021364:85021364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2396A>G |
| AA Mutation | p.Asn799Ser(p.N799S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 85020299:85020299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Gly740Arg(p.G740R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84867338:84867338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492C>T |
| AA Mutation | p.Pro498Ser(p.P498S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 85020320:85020320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2239T>G |
| AA Mutation | p.Phe747Val(p.F747V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84670887:84670887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.139G>A |
| AA Mutation | p.Asp47Asn(p.D47N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84727717:84727717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917C>T |
| AA Mutation | p.Thr306Ile(p.T306I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84707891:84707891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144037140 |
| CDS Mutation | c.407G>A |
| AA Mutation | p.Arg136His(p.R136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84752043:84752043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1354T>C |
| AA Mutation | p.Phe452Leu(p.F452L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84955420:84955420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2027A>T |
| AA Mutation | p.Asp676Val(p.D676V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323115 |
| Start | 84934273:84934273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1697A>C |
| AA Mutation | p.Lys566Thr(p.K566T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323115 |
| Start | 84867253:84867253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200550410 |
| CDS Mutation | c.1407C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |