Primary Site >> Stomach Cancer
Gene >> NFATC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79433701:79433701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1349C>G |
| AA Mutation | p.Ala450Gly(p.A450G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79527561:79527561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149271669 |
| CDS Mutation | c.2816C>T |
| AA Mutation | p.Thr939Met(p.T939M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410868:79410868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773868340 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Ala198Val(p.A198V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79527538:79527538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2793A>G |
| AA Mutation | p.Ile931Met(p.I931M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486279:79486279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2124T>G |
| AA Mutation | p.Asp708Glu(p.D708E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410667:79410667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.392A>G |
| AA Mutation | p.Asn131Ser(p.N131S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79448854:79448854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758037357 |
| CDS Mutation | c.1459C>T |
| AA Mutation | p.Arg487Cys(p.R487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79467522:79467522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753211496 |
| CDS Mutation | c.2032G>A |
| AA Mutation | p.Val678Ile(p.V678I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79411366:79411366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091C>G |
| AA Mutation | p.Ala364Gly(p.A364G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410705:79410705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769008406 |
| CDS Mutation | c.430G>A |
| AA Mutation | p.Val144Ile(p.V144I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410747:79410747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.472A>C |
| AA Mutation | p.Ser158Arg(p.S158R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410867:79410867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs180800829 |
| CDS Mutation | c.592G>A |
| AA Mutation | p.Ala198Thr(p.A198T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000427363 |
| Start | 79410976:79410976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753575733 |
| CDS Mutation | c.701C>T |
| AA Mutation | p.Pro234Leu(p.P234L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486792:79486792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763421772 |
| CDS Mutation | c.2637G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486402:79486402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201240540 |
| CDS Mutation | c.2247G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79451696:79451696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1783C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486927:79486927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2772C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79411052:79411052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374831399 |
| CDS Mutation | c.777C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79411139:79411139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200962841 |
| CDS Mutation | c.864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79448862:79448862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368496299 |
| CDS Mutation | c.1467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79433582:79433582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1230G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79451059:79451059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486762:79486762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763116408 |
| CDS Mutation | c.2607G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486607:79486607(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2456delC |
| AA Mutation | p.Pro819ArgfsTer8(p.P819Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000427363 |
| Start | 79486657:79486657(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774801875 |
| CDS Mutation | c.2507delC |
| AA Mutation | p.Pro836LeufsTer76(p.P836Lfs*76) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000427363 |
| Start | 79486529:79486529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2374C>T |
| AA Mutation | p.Gln792Ter(p.Q792*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |