Primary Site >> Stomach Cancer
Gene >> POLG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268124 |
| Start | 89320979:89320979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2768G>A |
| AA Mutation | p.Gly923Asp(p.G923D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268124 |
| Start | 89328959:89328959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1007C>T |
| AA Mutation | p.Ala336Val(p.A336V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268124 |
| Start | 89328705:89328705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1150G>A |
| AA Mutation | p.Asp384Asn(p.D384N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268124 |
| Start | 89317504:89317504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3515A>C |
| AA Mutation | p.Asp1172Ala(p.D1172A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268124 |
| Start | 89320856:89320856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767339769 |
| CDS Mutation | c.2891G>A |
| AA Mutation | p.Arg964His(p.R964H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89328778:89328778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1077G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89325677:89325677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1722G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89317488:89317488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89323850:89323850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373533550 |
| CDS Mutation | c.2122T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89321219:89321219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2640C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89318988:89318988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146936870 |
| CDS Mutation | c.3216C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268124 |
| Start | 89327213:89327213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1387T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268124 |
| Start | 89333208:89333208(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs35065786 |
| CDS Mutation | c.547delG |
| AA Mutation | p.Glu183ArgfsTer83(p.E183Rfs*83) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |