Primary Site >> Pancreatic Cancer
Gene >> MYO18B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 25823592:25823592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2609C>T |
| AA Mutation | p.Thr870Ile(p.T870I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 26026786:26026786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6812G>A |
| AA Mutation | p.Gly2271Asp(p.G2271D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 26027155:26027155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375762858 |
| CDS Mutation | c.7181C>T |
| AA Mutation | p.Ala2394Val(p.A2394V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 26027047:26027047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7073G>T |
| AA Mutation | p.Arg2358Ile(p.R2358I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 25769061:25769061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1145C>A |
| AA Mutation | p.Thr382Asn(p.T382N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 25823555:25823555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2572G>A |
| AA Mutation | p.Ala858Thr(p.A858T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 25950418:25950418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5800G>A |
| AA Mutation | p.Ala1934Thr(p.A1934T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 26003305:26003305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6328G>A |
| AA Mutation | p.Glu2110Lys(p.E2110K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 26027465:26027465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7491G>T |
| AA Mutation | p.Glu2497Asp(p.E2497D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000536101 |
| Start | 25768841:25768841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.925G>T |
| AA Mutation | p.Val309Leu(p.V309L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000536101 |
| Start | 25828954:25828954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2965C>T |
| AA Mutation | p.Gln989Ter(p.Q989*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000536101 |
| Start | 25952306:25952308(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5854_5856delATC |
| AA Mutation | p.Ile1952del(p.I1952del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |