Primary Site >> Stomach Cancer
Gene >> ZFAND4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626373:45626373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1450C>T |
| AA Mutation | p.His484Tyr(p.H484Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626183:45626183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1640G>A |
| AA Mutation | p.Arg547Gln(p.R547Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45627075:45627075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.748C>T |
| AA Mutation | p.Pro250Ser(p.P250S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626477:45626477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346T>C |
| AA Mutation | p.Leu449Pro(p.L449P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626318:45626318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1505T>C |
| AA Mutation | p.Leu502Pro(p.L502P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626439:45626439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140274256 |
| CDS Mutation | c.1384C>T |
| AA Mutation | p.Arg462Trp(p.R462W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626057:45626057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566283849 |
| CDS Mutation | c.1766G>A |
| AA Mutation | p.Gly589Asp(p.G589D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626520:45626520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1303T>A |
| AA Mutation | p.Leu435Met(p.L435M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45639907:45639907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.626C>T |
| AA Mutation | p.Ser209Phe(p.S209F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45618179:45618179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2009G>T |
| AA Mutation | p.Cys670Phe(p.C670F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45627029:45627029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559677417 |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Arg265His(p.R265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45626955:45626955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114572261 |
| CDS Mutation | c.868G>A |
| AA Mutation | p.Glu290Lys(p.E290K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45616480:45616480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759964148 |
| CDS Mutation | c.2140G>A |
| AA Mutation | p.Glu714Lys(p.E714K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344646 |
| Start | 45663577:45663577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149T>C |
| AA Mutation | p.Val50Ala(p.V50A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000344646 |
| Start | 45625952:45625952(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748928705 |
| CDS Mutation | c.1871delT |
| AA Mutation | p.Leu624CysfsTer8(p.L624Cfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344646 |
| Start | 45625977:45625977(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1846delC |
| AA Mutation | p.Gln616SerfsTer2(p.Q616Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |