Primary Site >> Stomach Cancer
Gene >> SPOCD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31814089:31814089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1245G>C |
| AA Mutation | p.Glu415Asp(p.E415D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31814723:31814723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611G>T |
| AA Mutation | p.Arg204Met(p.R204M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31814835:31814835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.499G>A |
| AA Mutation | p.Ala167Thr(p.A167T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31790902:31790902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777653631 |
| CDS Mutation | c.3352C>T |
| AA Mutation | p.Arg1118Cys(p.R1118C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31794157:31794157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2350C>T |
| AA Mutation | p.His784Tyr(p.H784Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31794227:31794227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2280G>T |
| AA Mutation | p.Gln760His(p.Q760H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31815261:31815261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.73C>T |
| AA Mutation | p.Leu25Phe(p.L25F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31800045:31800045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769296757 |
| CDS Mutation | c.1699G>A |
| AA Mutation | p.Asp567Asn(p.D567N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31815116:31815116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.218C>T |
| AA Mutation | p.Ala73Val(p.A73V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31793846:31793846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2435G>A |
| AA Mutation | p.Cys812Tyr(p.C812Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360482 |
| Start | 31799859:31799859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770934272 |
| CDS Mutation | c.1733G>A |
| AA Mutation | p.Gly578Asp(p.G578D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360482 |
| Start | 31798282:31798282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144387561 |
| CDS Mutation | c.2070C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360482 |
| Start | 31815048:31815048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.286C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360482 |
| Start | 31796680:31796680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146160927 |
| CDS Mutation | c.2181G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360482 |
| Start | 31791214:31791214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776119363 |
| CDS Mutation | c.3040C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |