Primary Site >> Stomach Cancer
Gene >> PTPRU
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29315440:29315440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3326G>A |
| AA Mutation | p.Gly1109Asp(p.G1109D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29259551:29259551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662G>A |
| AA Mutation | p.Arg221His(p.R221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29291943:29291943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2423G>A |
| AA Mutation | p.Arg808His(p.R808H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29323770:29323770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4124G>A |
| AA Mutation | p.Arg1375His(p.R1375H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29291978:29291978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149813959 |
| CDS Mutation | c.2458G>A |
| AA Mutation | p.Glu820Lys(p.E820K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29259527:29259527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.638C>T |
| AA Mutation | p.Ala213Val(p.A213V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29325253:29325253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4205G>A |
| AA Mutation | p.Cys1402Tyr(p.C1402Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000345512 |
| Start | 29279457:29279457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1565T>C |
| AA Mutation | p.Ile522Thr(p.I522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29325210:29325210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4162G>A |
| AA Mutation | p.Gly1388Ser(p.G1388S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29317796:29317796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3592G>A |
| AA Mutation | p.Ala1198Thr(p.A1198T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29291927:29291927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2407A>T |
| AA Mutation | p.Met803Leu(p.M803L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29255377:29255377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.176G>T |
| AA Mutation | p.Gly59Val(p.G59V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29311739:29311739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773999258 |
| CDS Mutation | c.3082C>T |
| AA Mutation | p.Arg1028Cys(p.R1028C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29315386:29315386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3272G>A |
| AA Mutation | p.Arg1091His(p.R1091H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29312657:29312657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374116935 |
| CDS Mutation | c.3208G>A |
| AA Mutation | p.Val1070Met(p.V1070M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29303971:29303971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144662614 |
| CDS Mutation | c.2623C>T |
| AA Mutation | p.Arg875Cys(p.R875C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29312658:29312658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3209T>C |
| AA Mutation | p.Val1070Ala(p.V1070A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29258559:29258559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.260T>C |
| AA Mutation | p.Val87Ala(p.V87A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345512 |
| Start | 29311740:29311740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759323710 |
| CDS Mutation | c.3083G>A |
| AA Mutation | p.Arg1028His(p.R1028H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345512 |
| Start | 29259504:29259504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370586274 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345512 |
| Start | 29255318:29255318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377643230 |
| CDS Mutation | c.117C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345512 |
| Start | 29320780:29320780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3813C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345512 |
| Start | 29312599:29312599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745686767 |
| CDS Mutation | c.3150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345512 |
| Start | 29303967:29303967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764110764 |
| CDS Mutation | c.2619G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |