Primary Site >> Stomach Cancer
Gene >> CPT1C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49705280:49705280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.946A>G |
| AA Mutation | p.Ile316Val(p.I316V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49707570:49707570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1396C>A |
| AA Mutation | p.Leu466Ile(p.L466I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49705990:49705990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151010811 |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Arg349Gln(p.R349Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49705232:49705232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Arg300Cys(p.R300C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49701549:49701549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753328360 |
| CDS Mutation | c.608C>T |
| AA Mutation | p.Ala203Val(p.A203V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49710387:49710387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1634T>A |
| AA Mutation | p.Val545Asp(p.V545D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49711833:49711833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539827461 |
| CDS Mutation | c.1891C>T |
| AA Mutation | p.Arg631Cys(p.R631C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49692284:49692284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.32G>A |
| AA Mutation | p.Arg11Gln(p.R11Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49710393:49710393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1640C>A |
| AA Mutation | p.Pro547Gln(p.P547Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49713501:49713501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2308C>T |
| AA Mutation | p.Arg770Cys(p.R770C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323446 |
| Start | 49711839:49711839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897G>A |
| AA Mutation | p.Ala633Thr(p.A633T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323446 |
| Start | 49705276:49705276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.942G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323446 |
| Start | 49701355:49701355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323446 |
| Start | 49692264:49692264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767198034 |
| CDS Mutation | c.12G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323446 |
| Start | 49697357:49697358(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.178dupC |
| AA Mutation | p.Leu60ProfsTer34(p.L60Pfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |