Primary Site >> Stomach Cancer
Gene >> SIAH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742280:150742280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758857423 |
| CDS Mutation | c.836C>T |
| AA Mutation | p.Thr279Met(p.T279M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742271:150742271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845C>T |
| AA Mutation | p.Ser282Leu(p.S282L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742668:150742668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448C>T |
| AA Mutation | p.His150Tyr(p.H150Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742335:150742335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.781T>G |
| AA Mutation | p.Phe261Val(p.F261V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742274:150742274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765846031 |
| CDS Mutation | c.842G>A |
| AA Mutation | p.Arg281His(p.R281H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150762639:150762639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.211C>G |
| AA Mutation | p.His71Asp(p.H71D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742301:150742301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543249698 |
| CDS Mutation | c.815G>A |
| AA Mutation | p.Arg272Gln(p.R272Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742503:150742503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613T>G |
| AA Mutation | p.Phe205Val(p.F205V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742626:150742626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Cys(p.R164C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742342:150742342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746804822 |
| CDS Mutation | c.774C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312960 |
| Start | 150742234:150742234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770915741 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312960 |
| Start | 150762514:150762514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312960 |
| Start | 150762517:150762517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765926111 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |