Primary Site >> Stomach Cancer
Gene >> IRX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749525:2749525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512G>A |
| AA Mutation | p.Arg171His(p.R171H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748554:2748554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1154C>T |
| AA Mutation | p.Thr385Met(p.T385M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748569:2748569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1139G>A |
| AA Mutation | p.Arg380His(p.R380H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749462:2749462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.575A>G |
| AA Mutation | p.Asp192Gly(p.D192G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748584:2748584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Ser375Leu(p.S375L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749427:2749427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610C>A |
| AA Mutation | p.Pro204Thr(p.P204T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749405:2749405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Thr211Met(p.T211M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749684:2749684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353G>C |
| AA Mutation | p.Arg118Pro(p.R118P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748914:2748914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.794A>C |
| AA Mutation | p.Asp265Ala(p.D265A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748405:2748405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1303G>A |
| AA Mutation | p.Gly435Ser(p.G435S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749409:2749409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765950888 |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Gly210Ser(p.G210S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749651:2749651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386T>C |
| AA Mutation | p.Leu129Pro(p.L129P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749722:2749722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748907:2748907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766887002 |
| CDS Mutation | c.801G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748511:2748511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749189949 |
| CDS Mutation | c.1197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748922:2748922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780600315 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2749386:2749386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748871:2748871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.837G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748841:2748841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.867C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302057 |
| Start | 2748472:2748472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767081175 |
| CDS Mutation | c.1236T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000302057 |
| Start | 2749005:2749005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.703G>T |
| AA Mutation | p.Glu235Ter(p.E235*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |