Primary Site >> Stomach Cancer
Gene >> FZD10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163871:130163871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.929C>T |
| AA Mutation | p.Thr310Met(p.T310M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163160:130163160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218C>T |
| AA Mutation | p.Pro73Leu(p.P73L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163556:130163556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614C>T |
| AA Mutation | p.Ala205Val(p.A205V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164120:130164120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1178C>T |
| AA Mutation | p.Ala393Val(p.A393V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163984:130163984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Glu348Lys(p.E348K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163389:130163389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.447G>T |
| AA Mutation | p.Glu149Asp(p.E149D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164167:130164167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1225G>A |
| AA Mutation | p.Gly409Ser(p.G409S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163073:130163073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131A>G |
| AA Mutation | p.Asp44Gly(p.D44G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164060:130164060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770701893 |
| CDS Mutation | c.1118G>A |
| AA Mutation | p.Arg373His(p.R373H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164275:130164275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1333G>A |
| AA Mutation | p.Gly445Arg(p.G445R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163255:130163255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778357040 |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Ala105Thr(p.A105T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163970:130163970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Gly343Asp(p.G343D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163483:130163483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.541C>G |
| AA Mutation | p.Pro181Ala(p.P181A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163378:130163378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436C>A |
| AA Mutation | p.Leu146Met(p.L146M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164269:130164269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1327C>T |
| AA Mutation | p.Arg443Cys(p.R443C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163843:130163843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.901C>A |
| AA Mutation | p.Gln301Lys(p.Q301K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163127:130163127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185G>A |
| AA Mutation | p.Arg62His(p.R62H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163696:130163696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Asp252Asn(p.D252N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164338:130164338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1396C>T |
| AA Mutation | p.Arg466Cys(p.R466C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163440:130163440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163578:130163578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758192337 |
| CDS Mutation | c.636G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164439:130164439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777850507 |
| CDS Mutation | c.1497C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164427:130164427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1485C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164673:130164673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1731G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164235:130164235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1293C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130164016:130164016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1074C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229030 |
| Start | 130163299:130163299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761092010 |
| CDS Mutation | c.357G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |