Primary Site >> Stomach Cancer
Gene >> AMPH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38394153:38394153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460C>T |
| AA Mutation | p.Ala487Val(p.A487V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38475352:38475352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.569A>G |
| AA Mutation | p.Glu190Gly(p.E190G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38466177:38466177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768225866 |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Ala221Val(p.A221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38384899:38384899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2007G>T |
| AA Mutation | p.Lys669Asn(p.K669N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38394193:38394193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1420G>A |
| AA Mutation | p.Asp474Asn(p.D474N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38491100:38491100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Gly116Arg(p.G116R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38475370:38475370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.551A>C |
| AA Mutation | p.Asn184Thr(p.N184T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38494485:38494485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.248A>T |
| AA Mutation | p.Glu83Val(p.E83V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38534963:38534963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781682680 |
| CDS Mutation | c.118G>A |
| AA Mutation | p.Glu40Lys(p.E40K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38463090:38463090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.773C>T |
| AA Mutation | p.Ala258Val(p.A258V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38491110:38491110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336A>C |
| AA Mutation | p.Lys112Asn(p.K112N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38494494:38494494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761049841 |
| CDS Mutation | c.239C>T |
| AA Mutation | p.Ser80Leu(p.S80L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38461372:38461372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.928A>T |
| AA Mutation | p.Thr310Ser(p.T310S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38384856:38384856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2050G>T |
| AA Mutation | p.Gly684Cys(p.G684C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38436365:38436365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041A>T |
| AA Mutation | p.Lys347Asn(p.K347N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38391918:38391918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748822925 |
| CDS Mutation | c.1708G>A |
| AA Mutation | p.Glu570Lys(p.E570K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356264 |
| Start | 38466174:38466174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665T>A |
| AA Mutation | p.Val222Glu(p.V222E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38394145:38394145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468G>A |
| AA Mutation | p.Glu490Lys(p.E490K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356264 |
| Start | 38466243:38466243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596T>C |
| AA Mutation | p.Val199Ala(p.V199A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356264 |
| Start | 38394035:38394035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1578A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356264 |
| Start | 38422466:38422466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1227T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356264 |
| Start | 38463074:38463074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148695925 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |