Primary Site >> Stomach Cancer
Gene >> CNGB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57901404:57901404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2924T>C |
| AA Mutation | p.Leu975Pro(p.L975P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897440:57897440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3199G>A |
| AA Mutation | p.Val1067Met(p.V1067M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897829:57897829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774186674 |
| CDS Mutation | c.3062C>T |
| AA Mutation | p.Thr1021Met(p.T1021M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57931731:57931731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1520C>T |
| AA Mutation | p.Ala507Val(p.A507V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897905:57897905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546596310 |
| CDS Mutation | c.2986G>A |
| AA Mutation | p.Gly996Ser(p.G996S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57931750:57931750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1501C>T |
| AA Mutation | p.Leu501Phe(p.L501F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57884183:57884183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3737G>T |
| AA Mutation | p.Arg1246Met(p.R1246M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57915322:57915322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2231G>T |
| AA Mutation | p.Ser744Ile(p.S744I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57916163:57916163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2183T>G |
| AA Mutation | p.Met728Arg(p.M728R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897822:57897822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3069A>C |
| AA Mutation | p.Lys1023Asn(p.K1023N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57919174:57919174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574295098 |
| CDS Mutation | c.1882G>A |
| AA Mutation | p.Asp628Asn(p.D628N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897496:57897496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755959274 |
| CDS Mutation | c.3143C>T |
| AA Mutation | p.Ala1048Val(p.A1048V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57884318:57884318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3602C>T |
| AA Mutation | p.Pro1201Leu(p.P1201L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57897511:57897511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200202348 |
| CDS Mutation | c.3128C>T |
| AA Mutation | p.Thr1043Met(p.T1043M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57884173:57884173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3747G>T |
| AA Mutation | p.Lys1249Asn(p.K1249N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251102 |
| Start | 57923336:57923336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78292723 |
| CDS Mutation | c.1580C>T |
| AA Mutation | p.Ala527Val(p.A527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251102 |
| Start | 57962980:57962980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251102 |
| Start | 57919121:57919121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251102 |
| Start | 57967149:57967149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753557311 |
| CDS Mutation | c.138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251102 |
| Start | 57904824:57904824(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768476420 |
| CDS Mutation | c.2544delG |
| AA Mutation | p.Leu849CysfsTer15(p.L849Cfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251102 |
| Start | 57960848:57960849(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.525dupA |
| AA Mutation | p.Ser176IlefsTer3(p.S176Ifs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251102 |
| Start | 57960851:57960852(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.522dupC |
| AA Mutation | p.Lys175GlnfsTer4(p.K175Qfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000251102 |
| Start | 57967295:57967295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.-8-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |