Primary Site >> Stomach Cancer
Gene >> MTA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105454218:105454218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.458A>G |
| AA Mutation | p.Tyr153Cys(p.Y153C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105470072:105470072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2005C>T |
| AA Mutation | p.Arg669Cys(p.R669C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105470151:105470151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782798640 |
| CDS Mutation | c.2084C>T |
| AA Mutation | p.Ala695Val(p.A695V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105470111:105470111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044C>T |
| AA Mutation | p.Arg682Cys(p.R682C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105464776:105464776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1447C>T |
| AA Mutation | p.Arg483Trp(p.R483W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105464118:105464118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1163G>A |
| AA Mutation | p.Gly388Glu(p.G388E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105470105:105470105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2038G>A |
| AA Mutation | p.Ala680Thr(p.A680T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105469488:105469488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835C>T |
| AA Mutation | p.Ala612Val(p.A612V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105470138:105470138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782366619 |
| CDS Mutation | c.2071C>T |
| AA Mutation | p.Arg691Cys(p.R691C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105460880:105460880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.869C>T |
| AA Mutation | p.Ala290Val(p.A290V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331320 |
| Start | 105464793:105464793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1464G>T |
| AA Mutation | p.Glu488Asp(p.E488D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331320 |
| Start | 105464122:105464122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1167T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331320 |
| Start | 105460920:105460920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781933559 |
| CDS Mutation | c.909T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |