Primary Site >> Stomach Cancer
Gene >> ZHX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952282:122952282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772G>A |
| AA Mutation | p.Val258Ile(p.V258I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122951889:122951889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758713483 |
| CDS Mutation | c.379G>A |
| AA Mutation | p.Asp127Asn(p.D127N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952806:122952806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1296G>T |
| AA Mutation | p.Lys432Asn(p.K432N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952349:122952349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839C>A |
| AA Mutation | p.Ser280Tyr(p.S280Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952463:122952463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.953G>A |
| AA Mutation | p.Gly318Asp(p.G318D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122953005:122953005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202088448 |
| CDS Mutation | c.1495G>A |
| AA Mutation | p.Val499Ile(p.V499I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952333:122952333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.823G>A |
| AA Mutation | p.Ala275Thr(p.A275T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952903:122952903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393G>T |
| AA Mutation | p.Asp465Tyr(p.D465Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952100:122952100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757779343 |
| CDS Mutation | c.590A>G |
| AA Mutation | p.Lys197Arg(p.K197R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952860:122952860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1350G>C |
| AA Mutation | p.Gln450His(p.Q450H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952768:122952768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762756401 |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Arg420Cys(p.R420C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952845:122952845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1335G>T |
| AA Mutation | p.Lys445Asn(p.K445N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122953991:122953991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751321473 |
| CDS Mutation | c.2481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122951912:122951912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761502245 |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952200:122952200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142739771 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952602:122952602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372060090 |
| CDS Mutation | c.1092G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122954006:122954006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749301737 |
| CDS Mutation | c.2496A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952050:122952050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.540G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314393 |
| Start | 122952815:122952815(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1310delC |
| AA Mutation | p.Pro437ArgfsTer15(p.P437Rfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000314393 |
| Start | 122953059:122953059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759681757 |
| CDS Mutation | c.1549C>T |
| AA Mutation | p.Arg517Ter(p.R517*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314393 |
| Start | 122953304:122953305(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1800dupA |
| AA Mutation | p.Gly601ArgfsTer71(p.G601Rfs*71) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |