Primary Site >> Stomach Cancer
Gene >> TP63
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189738725:189738725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275G>T |
| AA Mutation | p.Ser92Ile(p.S92I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189808513:189808513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.566C>T |
| AA Mutation | p.Ser189Leu(p.S189L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189894437:189894437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1978G>A |
| AA Mutation | p.Asp660Asn(p.D660N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189808362:189808362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Ala139Thr(p.A139T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189889412:189889412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580C>T |
| AA Mutation | p.Pro527Leu(p.P527L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264731 |
| Start | 189808525:189808525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.578C>T |
| AA Mutation | p.Thr193Met(p.T193M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264731 |
| Start | 189868714:189868714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143591434 |
| CDS Mutation | c.1127G>A |
| AA Mutation | p.Arg376His(p.R376H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189890793:189890793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1657T>A |
| AA Mutation | p.Leu553Ile(p.L553I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189886459:189886459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1415T>C |
| AA Mutation | p.Met472Thr(p.M472T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189866712:189866712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908849 |
| CDS Mutation | c.797G>A |
| AA Mutation | p.Arg266Gln(p.R266Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264731 |
| Start | 189864365:189864365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377757904 |
| CDS Mutation | c.713C>T |
| AA Mutation | p.Thr238Met(p.T238M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264731 |
| Start | 189808481:189808481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.534C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264731 |
| Start | 189808454:189808454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758433941 |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264731 |
| Start | 189866722:189866722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264731 |
| Start | 189866776:189866776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545050848 |
| CDS Mutation | c.861G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |