Primary Site >> Stomach Cancer
Gene >> TRAK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42223709:42223709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2834A>C |
| AA Mutation | p.Lys945Thr(p.K945T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202663:42202663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149693845 |
| CDS Mutation | c.1655G>A |
| AA Mutation | p.Arg552His(p.R552H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42223057:42223057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375388142 |
| CDS Mutation | c.2182C>T |
| AA Mutation | p.Arg728Cys(p.R728C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42194816:42194816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.988G>C |
| AA Mutation | p.Glu330Gln(p.E330Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42219574:42219574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044G>A |
| AA Mutation | p.Glu682Lys(p.E682K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202698:42202698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1690T>C |
| AA Mutation | p.Phe564Leu(p.F564L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42189024:42189024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.590G>A |
| AA Mutation | p.Arg197Lys(p.R197K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42219506:42219506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1976G>A |
| AA Mutation | p.Gly659Glu(p.G659E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202509:42202509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770373680 |
| CDS Mutation | c.1501C>T |
| AA Mutation | p.Arg501Trp(p.R501W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42219547:42219547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2017A>G |
| AA Mutation | p.Thr673Ala(p.T673A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42223120:42223120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2245A>G |
| AA Mutation | p.Ile749Val(p.I749V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327628 |
| Start | 42194807:42194807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.979C>T |
| AA Mutation | p.Arg327Cys(p.R327C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42223293:42223293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772671598 |
| CDS Mutation | c.2418C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42199206:42199206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764329895 |
| CDS Mutation | c.1143G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202691:42202691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1683C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202541:42202541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201849317 |
| CDS Mutation | c.1533G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42202745:42202745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757895013 |
| CDS Mutation | c.1737G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42209963:42209963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1941A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42125505:42125505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327628 |
| Start | 42223137:42223137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199845964 |
| CDS Mutation | c.2262C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |