Primary Site >> Stomach Cancer
Gene >> CYFIP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157325559:157325559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1978A>G |
| AA Mutation | p.Ile660Val(p.I660V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157359048:157359048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2792A>C |
| AA Mutation | p.Asn931Thr(p.N931T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157389258:157389258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3352G>A |
| AA Mutation | p.Glu1118Lys(p.E1118K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157304287:157304287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.716C>T |
| AA Mutation | p.Ala239Val(p.A239V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157341077:157341077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2668C>T |
| AA Mutation | p.Arg890Trp(p.R890W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157389205:157389205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3299G>A |
| AA Mutation | p.Arg1100His(p.R1100H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157389375:157389375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369611074 |
| CDS Mutation | c.3469G>A |
| AA Mutation | p.Ala1157Thr(p.A1157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157300735:157300735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.408C>A |
| AA Mutation | p.Phe136Leu(p.F136L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157383304:157383304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3227C>T |
| AA Mutation | p.Ala1076Val(p.A1076V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157307831:157307831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.866G>T |
| AA Mutation | p.Arg289Ile(p.R289I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157320676:157320676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1545G>T |
| AA Mutation | p.Lys515Asn(p.K515N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157359107:157359107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2851G>A |
| AA Mutation | p.Ala951Thr(p.A951T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157311728:157311728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1057C>T |
| AA Mutation | p.Arg353Trp(p.R353W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157315087:157315087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1349T>G |
| AA Mutation | p.Phe450Cys(p.F450C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157339126:157339126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2530A>G |
| AA Mutation | p.Ser844Gly(p.S844G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157294840:157294840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.265T>G |
| AA Mutation | p.Cys89Gly(p.C89G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157389330:157389330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764457342 |
| CDS Mutation | c.3424G>A |
| AA Mutation | p.Val1142Ile(p.V1142I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616178 |
| Start | 157319864:157319864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1459G>A |
| AA Mutation | p.Ala487Thr(p.A487T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616178 |
| Start | 157328020:157328020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2202C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616178 |
| Start | 157325555:157325555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1974A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616178 |
| Start | 157389386:157389386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267600516 |
| CDS Mutation | c.3480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |