Primary Site >> Stomach Cancer
Gene >> KRT16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611458:41611458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.658G>A |
| AA Mutation | p.Val220Ile(p.V220I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611101:41611101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.901C>A |
| AA Mutation | p.Arg301Ser(p.R301S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611469:41611469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.647T>C |
| AA Mutation | p.Val216Ala(p.V216A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611696:41611696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547733077 |
| CDS Mutation | c.557C>T |
| AA Mutation | p.Ala186Val(p.A186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41610358:41610358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777901534 |
| CDS Mutation | c.1253G>A |
| AA Mutation | p.Arg418His(p.R418H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41612195:41612195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Ser165Asn(p.S165N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41612262:41612262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Ala143Thr(p.A143T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41609987:41609987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1370C>A |
| AA Mutation | p.Pro457His(p.P457H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611415:41611415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701G>A |
| AA Mutation | p.Arg234Lys(p.R234K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611451:41611451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665G>A |
| AA Mutation | p.Gly222Asp(p.G222D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611090:41611090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301653 |
| Start | 41611165:41611165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368580381 |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000301653 |
| Start | 41610544:41610545(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1066_1067insTTGTTGCCTATTAAAGG |
| AA Mutation | p.Ser356PhefsTer5(p.S356Ffs*5) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301653 |
| Start | 41610543:41610544(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1067_1068insTGTTGGT |
| AA Mutation | p.Leu357ValfsTer38(p.L357Vfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |