Primary Site >> Stomach Cancer
Gene >> NFATC4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24369576:24369576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178G>A |
| AA Mutation | p.Gly60Ser(p.G60S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24374430:24374430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1837C>T |
| AA Mutation | p.Pro613Ser(p.P613S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24373289:24373289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1478C>T |
| AA Mutation | p.Ala493Val(p.A493V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24372586:24372586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756073934 |
| CDS Mutation | c.1342G>A |
| AA Mutation | p.Gly448Ser(p.G448S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24369520:24369520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Pro41Leu(p.P41L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24369633:24369633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Ala79Thr(p.A79T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24373787:24373787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1652G>A |
| AA Mutation | p.Arg551Gln(p.R551Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24370074:24370074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676A>T |
| AA Mutation | p.Thr226Ser(p.T226S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24376828:24376828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2591G>A |
| AA Mutation | p.Ser864Asn(p.S864N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24376473:24376473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2236C>T |
| AA Mutation | p.Pro746Ser(p.P746S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24370209:24370209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811T>C |
| AA Mutation | p.Tyr271His(p.Y271H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24376318:24376318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756648728 |
| CDS Mutation | c.2081C>T |
| AA Mutation | p.Pro694Leu(p.P694L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24376059:24376059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748592990 |
| CDS Mutation | c.2014C>T |
| AA Mutation | p.Arg672Trp(p.R672W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24373288:24373288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1477G>A |
| AA Mutation | p.Ala493Thr(p.A493T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000250373 |
| Start | 24370255:24370255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857G>A |
| AA Mutation | p.Arg286His(p.R286H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250373 |
| Start | 24373854:24373854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1719G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250373 |
| Start | 24376583:24376583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2346C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000250373 |
| Start | 24374363:24374363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1770C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250373 |
| Start | 24374348:24374357(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1756_1765delCCCCAGGTGG |
| AA Mutation | p.Pro586ArgfsTer10(p.P586Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000250373 |
| Start | 24369884:24369885(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs751744912 |
| CDS Mutation | c.493dupG |
| AA Mutation | p.Ala165GlyfsTer23(p.A165Gfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |