Primary Site >> Stomach Cancer
Gene >> MCM2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127620871:127620871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2439C>G |
| AA Mutation | p.Ser813Arg(p.S813R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127619145:127619145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2132G>A |
| AA Mutation | p.Gly711Asp(p.G711D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127604723:127604723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.352C>T |
| AA Mutation | p.Arg118Trp(p.R118W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127608487:127608487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1207G>A |
| AA Mutation | p.Val403Met(p.V403M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127608908:127608908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1313T>A |
| AA Mutation | p.Val438Asp(p.V438D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265056 |
| Start | 127615953:127615953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1520C>G |
| AA Mutation | p.Pro507Arg(p.P507R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127620866:127620866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766565920 |
| CDS Mutation | c.2434C>T |
| AA Mutation | p.Arg812Cys(p.R812C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127617018:127617018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768309904 |
| CDS Mutation | c.1673C>T |
| AA Mutation | p.Ala558Val(p.A558V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127604976:127604976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566433714 |
| CDS Mutation | c.493G>A |
| AA Mutation | p.Glu165Lys(p.E165K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127621173:127621173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770365114 |
| CDS Mutation | c.2549G>A |
| AA Mutation | p.Arg850His(p.R850H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127619220:127619220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2207A>G |
| AA Mutation | p.Asn736Ser(p.N736S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127621103:127621103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2479G>A |
| AA Mutation | p.Asp827Asn(p.D827N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127620876:127620876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779228557 |
| CDS Mutation | c.2444G>A |
| AA Mutation | p.Arg815His(p.R815H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127616997:127616997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781253937 |
| CDS Mutation | c.1652C>T |
| AA Mutation | p.Ala551Val(p.A551V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127621167:127621167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137990158 |
| CDS Mutation | c.2543G>A |
| AA Mutation | p.Arg848His(p.R848H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265056 |
| Start | 127617068:127617068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Ala575Thr(p.A575T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127606784:127606784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1068G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127604617:127604617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186022338 |
| CDS Mutation | c.246C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127604704:127604704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127609014:127609014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757423043 |
| CDS Mutation | c.1419C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127617019:127617019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376837416 |
| CDS Mutation | c.1674G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265056 |
| Start | 127619212:127619212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144817363 |
| CDS Mutation | c.2199G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |