Primary Site >> Stomach Cancer
Gene >> SGCE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94623378:94623378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548306335 |
| CDS Mutation | c.410G>A |
| AA Mutation | p.Arg137His(p.R137H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94603366:94603366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.749A>C |
| AA Mutation | p.Gln250Pro(p.Q250P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94598841:94598841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1187A>G |
| AA Mutation | p.Glu396Gly(p.E396G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94656059:94656059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763973436 |
| CDS Mutation | c.40G>A |
| AA Mutation | p.Ala14Thr(p.A14T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94656016:94656016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.83C>T |
| AA Mutation | p.Ala28Val(p.A28V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94628260:94628260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.332A>G |
| AA Mutation | p.Asp111Gly(p.D111G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265735 |
| Start | 94628353:94628353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.239T>C |
| AA Mutation | p.Ile80Thr(p.I80T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265735 |
| Start | 94603422:94603422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757206832 |
| CDS Mutation | c.693G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265735 |
| Start | 94628355:94628355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.237G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |