Primary Site >> Stomach Cancer
Gene >> GAN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81365442:81365442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1466C>T |
| AA Mutation | p.Thr489Ile(p.T489I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81354507:81354507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385A>G |
| AA Mutation | p.Ile129Val(p.I129V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81365397:81365397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1421G>T |
| AA Mutation | p.Gly474Val(p.G474V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81354615:81354615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493A>G |
| AA Mutation | p.Ser165Gly(p.S165G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81354480:81354480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.358C>A |
| AA Mutation | p.Leu120Met(p.L120M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81377525:81377525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780683261 |
| CDS Mutation | c.1723A>G |
| AA Mutation | p.Ile575Val(p.I575V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000568107 |
| Start | 81356902:81356902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749359745 |
| CDS Mutation | c.751A>G |
| AA Mutation | p.Ile251Val(p.I251V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000568107 |
| Start | 81365425:81365425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1449G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000568107 |
| Start | 81365362:81365362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1386G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000568107 |
| Start | 81377255:81377255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774396975 |
| CDS Mutation | c.1539C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |