Primary Site >> Stomach Cancer
Gene >> IL12RB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67395826:67395826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774704366 |
| CDS Mutation | c.2326G>A |
| AA Mutation | p.Asp776Asn(p.D776N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67338688:67338688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749883157 |
| CDS Mutation | c.1023T>G |
| AA Mutation | p.Ile341Met(p.I341M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67350900:67350900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1069A>C |
| AA Mutation | p.Ile357Leu(p.I357L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67386597:67386597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1874C>A |
| AA Mutation | p.Ala625Glu(p.A625E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67395757:67395757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2257C>A |
| AA Mutation | p.Pro753Thr(p.P753T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67395860:67395860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141507006 |
| CDS Mutation | c.2360C>T |
| AA Mutation | p.Thr787Met(p.T787M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67329629:67329629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707A>C |
| AA Mutation | p.Lys236Thr(p.K236T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67328247:67328247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527T>G |
| AA Mutation | p.Ile176Ser(p.I176S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67395952:67395952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2452T>A |
| AA Mutation | p.Ser818Thr(p.S818T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67329701:67329701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771299847 |
| CDS Mutation | c.779G>A |
| AA Mutation | p.Arg260Gln(p.R260Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67372667:67372667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1601A>G |
| AA Mutation | p.Lys534Arg(p.K534R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262345 |
| Start | 67386597:67386597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2307154 |
| CDS Mutation | c.1874C>T |
| AA Mutation | p.Ala625Val(p.A625V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262345 |
| Start | 67395912:67395912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2412C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262345 |
| Start | 67372485:67372485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771180528 |
| CDS Mutation | c.1509A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262345 |
| Start | 67320423:67320423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262345 |
| Start | 67390104:67390104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373096534 |
| CDS Mutation | c.2022C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |