Primary Site >> Stomach Cancer
Gene >> PTPRC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198734369:198734369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2221T>C |
| AA Mutation | p.Trp741Arg(p.W741R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198716795:198716795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1405C>T |
| AA Mutation | p.Arg469Cys(p.R469C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198734416:198734416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2268A>C |
| AA Mutation | p.Glu756Asp(p.E756D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198732369:198732369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044C>T |
| AA Mutation | p.Arg682Cys(p.R682C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198718259:198718259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1616T>C |
| AA Mutation | p.Phe539Ser(p.F539S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198709729:198709729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1076T>G |
| AA Mutation | p.Leu359Arg(p.L359R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198696895:198696895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.284C>T |
| AA Mutation | p.Ala95Val(p.A95V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198639335:198639335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67G>A |
| AA Mutation | p.Val23Met(p.V23M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198718253:198718253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1610G>T |
| AA Mutation | p.Cys537Phe(p.C537F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198696867:198696867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256T>A |
| AA Mutation | p.Ser86Thr(p.S86T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198754301:198754301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3542C>A |
| AA Mutation | p.Ala1181Asp(p.A1181D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198716813:198716813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1423A>T |
| AA Mutation | p.Met475Leu(p.M475L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198742361:198742361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2691A>C |
| AA Mutation | p.Gln897His(p.Q897H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198742361:198742361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2691A>T |
| AA Mutation | p.Gln897His(p.Q897H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198718255:198718255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144856406 |
| CDS Mutation | c.1612G>A |
| AA Mutation | p.Asp538Asn(p.D538N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198716747:198716747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1357A>C |
| AA Mutation | p.Thr453Pro(p.T453P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442510 |
| Start | 198716775:198716775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1385A>C |
| AA Mutation | p.Tyr462Ser(p.Y462S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198750576:198750576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3157A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198709793:198709793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200643724 |
| CDS Mutation | c.1140C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198742361:198742361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2691A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198712960:198712960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1179A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198741910:198741910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2445G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198732547:198732547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776208869 |
| CDS Mutation | c.2133C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198706885:198706885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137909392 |
| CDS Mutation | c.837G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442510 |
| Start | 198718242:198718242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372045826 |
| CDS Mutation | c.1599G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |