Primary Site >> Stomach Cancer
Gene >> SOGA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36816157:36816157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773787300 |
| CDS Mutation | c.1285G>A |
| AA Mutation | p.Ala429Thr(p.A429T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36808573:36808573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760059295 |
| CDS Mutation | c.2754G>C |
| AA Mutation | p.Trp918Cys(p.W918C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36816278:36816278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1164G>T |
| AA Mutation | p.Leu388Phe(p.L388F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000237536 |
| Start | 36808742:36808742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2585T>G |
| AA Mutation | p.Leu862Arg(p.L862R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36794565:36794565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3517A>G |
| AA Mutation | p.Ser1173Gly(p.S1173G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36802956:36802956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3239G>A |
| AA Mutation | p.Arg1080His(p.R1080H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36815338:36815338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2104G>A |
| AA Mutation | p.Glu702Lys(p.E702K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36794384:36794384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3698C>T |
| AA Mutation | p.Pro1233Leu(p.P1233L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36815634:36815634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1808G>A |
| AA Mutation | p.Arg603His(p.R603H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36839338:36839338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.791C>T |
| AA Mutation | p.Ala264Val(p.A264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237536 |
| Start | 36839407:36839407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722A>G |
| AA Mutation | p.Glu241Gly(p.E241G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237536 |
| Start | 36815927:36815927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773270451 |
| CDS Mutation | c.1515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237536 |
| Start | 36816158:36816158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555074017 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |