Primary Site >> Stomach Cancer
Gene >> AGAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57734645:57734645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1262C>T |
| AA Mutation | p.Ser421Leu(p.S421L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57730836:57730836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2263G>A |
| AA Mutation | p.Gly755Arg(p.G755R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57727049:57727049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3261G>T |
| AA Mutation | p.Glu1087Asp(p.E1087D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57727768:57727768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2770C>T |
| AA Mutation | p.Arg924Cys(p.R924C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57731958:57731958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771629262 |
| CDS Mutation | c.1804G>A |
| AA Mutation | p.Gly602Arg(p.G602R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57732416:57732416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138992134 |
| CDS Mutation | c.1781C>T |
| AA Mutation | p.Pro594Leu(p.P594L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57730856:57730856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2243G>A |
| AA Mutation | p.Gly748Asp(p.G748D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000547588 |
| Start | 57730848:57730848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2251G>A |
| AA Mutation | p.Ala751Thr(p.A751T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000547588 |
| Start | 57728063:57728063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752551386 |
| CDS Mutation | c.2640C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000547588 |
| Start | 57730837:57730837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147633851 |
| CDS Mutation | c.2262C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000547588 |
| Start | 57731944:57731944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201319391 |
| CDS Mutation | c.1818C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |