Primary Site >> Stomach Cancer
Gene >> ROR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64177472:64177472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1431A>C |
| AA Mutation | p.Glu477Asp(p.E477D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64049835:64049835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200761925 |
| CDS Mutation | c.308G>A |
| AA Mutation | p.Arg103Gln(p.R103Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64049879:64049879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.352A>G |
| AA Mutation | p.Ile118Val(p.I118V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371079 |
| Start | 64142650:64142650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1174G>A |
| AA Mutation | p.Asp392Asn(p.D392N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64178438:64178438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2397G>T |
| AA Mutation | p.Gln799His(p.Q799H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64178464:64178464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551069295 |
| CDS Mutation | c.2423C>T |
| AA Mutation | p.Pro808Leu(p.P808L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64140271:64140271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.773T>A |
| AA Mutation | p.Val258Asp(p.V258D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64049753:64049753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.226G>C |
| AA Mutation | p.Glu76Gln(p.E76Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64177761:64177761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1720G>A |
| AA Mutation | p.Gly574Ser(p.G574S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64142449:64142449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150545478 |
| CDS Mutation | c.973G>A |
| AA Mutation | p.Val325Ile(p.V325I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64178205:64178205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2164T>C |
| AA Mutation | p.Tyr722His(p.Y722H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64142480:64142480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1004A>G |
| AA Mutation | p.Gln335Arg(p.Q335R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371079 |
| Start | 64140231:64140231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528483506 |
| CDS Mutation | c.733C>T |
| AA Mutation | p.Arg245Cys(p.R245C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371079 |
| Start | 64159084:64159084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149862457 |
| CDS Mutation | c.1278C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |