Primary Site >> Stomach Cancer
Gene >> TTC37
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95516566:95516566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2536G>A |
| AA Mutation | p.Ala846Thr(p.A846T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95543287:95543287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.131T>G |
| AA Mutation | p.Val44Gly(p.V44G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95516948:95516948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2404G>A |
| AA Mutation | p.Asp802Asn(p.D802N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95528078:95528078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1069G>A |
| AA Mutation | p.Ala357Thr(p.A357T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95540821:95540821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412A>T |
| AA Mutation | p.Thr138Ser(p.T138S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95490967:95490967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3872A>G |
| AA Mutation | p.Asn1291Ser(p.N1291S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95522142:95522142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1923A>G |
| AA Mutation | p.Ile641Met(p.I641M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95522262:95522262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1803G>T |
| AA Mutation | p.Trp601Cys(p.W601C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95467887:95467887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4599A>C |
| AA Mutation | p.Lys1533Asn(p.K1533N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95513606:95513606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2743G>A |
| AA Mutation | p.Asp915Asn(p.D915N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95528023:95528023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201518366 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Thr375Met(p.T375M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95484794:95484794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3983C>A |
| AA Mutation | p.Ser1328Tyr(p.S1328Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358746 |
| Start | 95516746:95516746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2441T>C |
| AA Mutation | p.Leu814Pro(p.L814P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358746 |
| Start | 95502996:95502996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3225G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358746 |
| Start | 95523742:95523742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1545A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358746 |
| Start | 95482511:95482511(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4174delA |
| AA Mutation | p.Thr1392GlnfsTer24(p.T1392Qfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358746 |
| Start | 95543223:95543223(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751628166 |
| CDS Mutation | c.195delA |
| AA Mutation | p.Ala66LeufsTer4(p.A66Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |