Primary Site >> Stomach Cancer
Gene >> KLHL6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183492508:183492508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757613109 |
| CDS Mutation | c.1550G>A |
| AA Mutation | p.Arg517His(p.R517H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183555380:183555380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776911567 |
| CDS Mutation | c.274G>A |
| AA Mutation | p.Ala92Thr(p.A92T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183555457:183555457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197G>A |
| AA Mutation | p.Arg66Gln(p.R66Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183492060:183492060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1733G>A |
| AA Mutation | p.Cys578Tyr(p.C578Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183494197:183494197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1232G>T |
| AA Mutation | p.Arg411Leu(p.R411L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183499754:183499754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372412048 |
| CDS Mutation | c.983C>T |
| AA Mutation | p.Thr328Met(p.T328M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183491967:183491967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1826C>T |
| AA Mutation | p.Thr609Ile(p.T609I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183508147:183508147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535540527 |
| CDS Mutation | c.821C>T |
| AA Mutation | p.Thr274Met(p.T274M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183555446:183555446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749942087 |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Ala70Thr(p.A70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341319 |
| Start | 183555442:183555442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212T>C |
| AA Mutation | p.Leu71Pro(p.L71P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341319 |
| Start | 183527872:183527872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.432G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341319 |
| Start | 183492068:183492068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1725G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341319 |
| Start | 183499621:183499621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149326068 |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |