Primary Site >> Stomach Cancer
Gene >> ARAP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141669804:141669804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2257T>C |
| AA Mutation | p.Phe753Leu(p.F753L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141659413:141659413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3331G>A |
| AA Mutation | p.Val1111Met(p.V1111M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141672603:141672603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1334G>A |
| AA Mutation | p.Arg445Gln(p.R445Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141671718:141671718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146818768 |
| CDS Mutation | c.1706G>A |
| AA Mutation | p.Arg569His(p.R569H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141665036:141665036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554504713 |
| CDS Mutation | c.2686G>A |
| AA Mutation | p.Ala896Thr(p.A896T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141671387:141671387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1868C>A |
| AA Mutation | p.Ala623Asp(p.A623D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000239440 |
| Start | 141671895:141671895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1671G>T |
| AA Mutation | p.Gln557His(p.Q557H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141670578:141670578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2041G>A |
| AA Mutation | p.Gly681Ser(p.G681S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141671946:141671946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1620G>T |
| AA Mutation | p.Lys540Asn(p.K540N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141656218:141656218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758532450 |
| CDS Mutation | c.3848G>A |
| AA Mutation | p.Arg1283His(p.R1283H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239440 |
| Start | 141654302:141654302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375260150 |
| CDS Mutation | c.4283C>T |
| AA Mutation | p.Thr1428Ile(p.T1428I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239440 |
| Start | 141672220:141672220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149846650 |
| CDS Mutation | c.1467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239440 |
| Start | 141673017:141673017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146992507 |
| CDS Mutation | c.1089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000239440 |
| Start | 141672253:141672253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753023119 |
| CDS Mutation | c.1434G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |