Primary Site >> Stomach Cancer
Gene >> COL1A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94423077:94423077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2524T>G |
| AA Mutation | p.Phe842Val(p.F842V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94423091:94423091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2538G>T |
| AA Mutation | p.Lys846Asn(p.K846N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94412102:94412102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1385C>T |
| AA Mutation | p.Ala462Val(p.A462V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94423018:94423018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1800240 |
| CDS Mutation | c.2465G>A |
| AA Mutation | p.Arg822His(p.R822H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94399077:94399077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125G>T |
| AA Mutation | p.Gly42Val(p.G42V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427236:94427236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3208C>A |
| AA Mutation | p.His1070Asn(p.H1070N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94416411:94416411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1771C>T |
| AA Mutation | p.Arg591Cys(p.R591C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94408809:94408809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Ala260Thr(p.A260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94413924:94413924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642C>T |
| AA Mutation | p.Pro548Ser(p.P548S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427823:94427823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3464C>A |
| AA Mutation | p.Ser1155Tyr(p.S1155Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427761:94427761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3402A>T |
| AA Mutation | p.Glu1134Asp(p.E1134D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94410273:94410273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1067A>T |
| AA Mutation | p.Glu356Val(p.E356V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94426046:94426046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2992C>G |
| AA Mutation | p.Pro998Ala(p.P998A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94425628:94425628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2800G>A |
| AA Mutation | p.Gly934Ser(p.G934S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427761:94427761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3402A>C |
| AA Mutation | p.Glu1134Asp(p.E1134D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94409768:94409768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs66612022 |
| CDS Mutation | c.982G>A |
| AA Mutation | p.Gly328Ser(p.G328S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94404867:94404867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407G>A |
| AA Mutation | p.Gly136Asp(p.G136D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94400259:94400259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.196G>T |
| AA Mutation | p.Gly66Cys(p.G66C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94425759:94425759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72659312 |
| CDS Mutation | c.2845G>A |
| AA Mutation | p.Gly949Ser(p.G949S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427751:94427751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3392A>C |
| AA Mutation | p.Lys1131Thr(p.K1131T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297268 |
| Start | 94405252:94405252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.486G>T |
| AA Mutation | p.Gln162His(p.Q162H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427628:94427628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267606742 |
| CDS Mutation | c.3269G>A |
| AA Mutation | p.Gly1090Asp(p.G1090D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94429373:94429373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3897A>C |
| AA Mutation | p.Glu1299Asp(p.E1299D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94430320:94430320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4028A>C |
| AA Mutation | p.Asp1343Ala(p.D1343A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94430322:94430322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4030A>T |
| AA Mutation | p.Ile1344Phe(p.I1344F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94423099:94423099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2546C>G |
| AA Mutation | p.Ser849Cys(p.S849C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94428334:94428334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3568G>A |
| AA Mutation | p.Ala1190Thr(p.A1190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297268 |
| Start | 94425136:94425136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2693G>A |
| AA Mutation | p.Gly898Asp(p.G898D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427695:94427695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34691365 |
| CDS Mutation | c.3336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94425654:94425654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199580542 |
| CDS Mutation | c.2826C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427055:94427055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3153T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94408796:94408796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.765A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427647:94427647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149097024 |
| CDS Mutation | c.3288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94418504:94418504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1977A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297268 |
| Start | 94412094:94412094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770230919 |
| CDS Mutation | c.1377C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297268 |
| Start | 94426471:94426472(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3047_3048delCC |
| AA Mutation | p.Pro1016GlnfsTer24(p.P1016Qfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297268 |
| Start | 94427755:94427756(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3397_3401dupTATGA |
| AA Mutation | p.Glu1134AspfsTer8(p.E1134Dfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297268 |
| Start | 94421055:94421056(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2348dupC |
| AA Mutation | p.Gly784TrpfsTer41(p.G784Wfs*41) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |