Primary Site >> Stomach Cancer
Gene >> RGS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113479496:113479496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421C>A |
| AA Mutation | p.Leu141Met(p.L141M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113584323:113584323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2911G>T |
| AA Mutation | p.Ala971Ser(p.A971S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113507357:113507357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749765337 |
| CDS Mutation | c.1156G>A |
| AA Mutation | p.Gly386Arg(p.G386R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113484189:113484189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770598136 |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Val193Ile(p.V193I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113505512:113505512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ala323Val(p.A323V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113507594:113507594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393G>A |
| AA Mutation | p.Asp465Asn(p.D465N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113507462:113507462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772034212 |
| CDS Mutation | c.1261C>T |
| AA Mutation | p.Arg421Cys(p.R421C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113596829:113596829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3473G>A |
| AA Mutation | p.Gly1158Asp(p.G1158D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113461727:113461727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.101C>A |
| AA Mutation | p.Pro34His(p.P34H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113514619:113514619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Ala547Thr(p.A547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113514484:113514484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1504T>C |
| AA Mutation | p.Ser502Pro(p.S502P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113591351:113591351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750641666 |
| CDS Mutation | c.3034G>A |
| AA Mutation | p.Val1012Ile(p.V1012I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350696 |
| Start | 113594498:113594498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374543370 |
| CDS Mutation | c.3149C>T |
| AA Mutation | p.Ala1050Val(p.A1050V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350696 |
| Start | 113595621:113595621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3267C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350696 |
| Start | 113584232:113584232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2820G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350696 |
| Start | 113596881:113596881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370256072 |
| CDS Mutation | c.3525G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350696 |
| Start | 113595705:113595705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3351G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350696 |
| Start | 113584220:113584220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755732596 |
| CDS Mutation | c.2808G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |