Primary Site >> Stomach Cancer
Gene >> TRPV6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142877958:142877958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197A>G |
| AA Mutation | p.Lys66Arg(p.K66R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142875771:142875771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.896C>T |
| AA Mutation | p.Thr299Ile(p.T299I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142885480:142885480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.37C>A |
| AA Mutation | p.Leu13Ile(p.L13I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142875541:142875541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049G>A |
| AA Mutation | p.Arg350His(p.R350H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142871879:142871879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2006T>G |
| AA Mutation | p.Leu669Arg(p.L669R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142873579:142873579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657T>G |
| AA Mutation | p.Phe553Val(p.F553V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142877214:142877214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141260669 |
| CDS Mutation | c.415C>T |
| AA Mutation | p.Arg139Cys(p.R139C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142871714:142871714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2171A>G |
| AA Mutation | p.Gln724Arg(p.Q724R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142877951:142877951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199805481 |
| CDS Mutation | c.204G>T |
| AA Mutation | p.Glu68Asp(p.E68D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359396 |
| Start | 142873573:142873573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1663T>C |
| AA Mutation | p.Tyr555His(p.Y555H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359396 |
| Start | 142873562:142873562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1674C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_retained_variant |
| Transcription ID | ENST00000359396 |
| Start | 142871708:142871708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2177G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359396 |
| Start | 142876504:142876504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138217574 |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359396 |
| Start | 142876455:142876455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Gln239Ter(p.Q239*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |