Primary Site >> Stomach Cancer
Gene >> CCNL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390804:1390804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.721G>A |
| AA Mutation | p.Ala241Thr(p.A241T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1393455:1393455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.600C>G |
| AA Mutation | p.Ile200Met(p.I200M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390233:1390233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1003C>A |
| AA Mutation | p.Leu335Met(p.L335M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390326:1390326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746945804 |
| CDS Mutation | c.910G>A |
| AA Mutation | p.Ala304Thr(p.A304T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390839:1390839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.686C>T |
| AA Mutation | p.Thr229Ile(p.T229I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1387404:1387404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751164412 |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Arg464Trp(p.R464W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | coding_sequence_variant;3_prime_UTR_variant |
| Transcription ID | ENST00000400809 |
| Start | 1387229:1387237(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1557_*2delGAGGTGAGG |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1398622:1398622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338A>T |
| AA Mutation | p.Lys113Met(p.K113M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400809 |
| Start | 1398332:1398332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.374T>C |
| AA Mutation | p.Met125Thr(p.M125T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400809 |
| Start | 1395424:1395424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.564T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390829:1390829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763255792 |
| CDS Mutation | c.696C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400809 |
| Start | 1395508:1395508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552669870 |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000400809 |
| Start | 1390460:1390460(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.863delA |
| AA Mutation | p.Lys288ArgfsTer65(p.K288Rfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000400809 |
| Start | 1387314:1387314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749300030 |
| CDS Mutation | c.1480C>T |
| AA Mutation | p.Arg494Ter(p.R494*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |