Primary Site >> Stomach Cancer
Gene >> PNPLA6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7560730:7560730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3812G>A |
| AA Mutation | p.Arg1271Gln(p.R1271Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7540984:7540984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Arg295His(p.R295H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7559063:7559063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3641T>G |
| AA Mutation | p.Val1214Gly(p.V1214G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7559095:7559095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3673C>T |
| AA Mutation | p.Arg1225Cys(p.R1225C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7543044:7543044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595A>G |
| AA Mutation | p.His532Arg(p.H532R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7555749:7555749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3109C>T |
| AA Mutation | p.Arg1037Trp(p.R1037W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7540675:7540675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587777184 |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Val263Ile(p.V263I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7556490:7556490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3161C>T |
| AA Mutation | p.Thr1054Met(p.T1054M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7559125:7559125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3703G>A |
| AA Mutation | p.Asp1235Asn(p.D1235N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7558888:7558888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3466G>A |
| AA Mutation | p.Ala1156Thr(p.A1156T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7550389:7550389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1933A>G |
| AA Mutation | p.Ile645Val(p.I645V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7542644:7542644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573529919 |
| CDS Mutation | c.1363G>A |
| AA Mutation | p.Gly455Arg(p.G455R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000414982 |
| Start | 7542669:7542669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370626406 |
| CDS Mutation | c.1388G>A |
| AA Mutation | p.Arg463Gln(p.R463Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7551365:7551365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2215G>A |
| AA Mutation | p.Val739Met(p.V739M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7550561:7550561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2018G>A |
| AA Mutation | p.Arg673Gln(p.R673Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7557179:7557179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3322C>T |
| AA Mutation | p.Arg1108Trp(p.R1108W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000414982 |
| Start | 7550070:7550070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1799G>A |
| AA Mutation | p.Arg600His(p.R600H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000414982 |
| Start | 7554982:7554982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2754C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000414982 |
| Start | 7561037:7561037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3870C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000414982 |
| Start | 7541027:7541027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757524146 |
| CDS Mutation | c.927G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000414982 |
| Start | 7558995:7558995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3573A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000414982 |
| Start | 7561284:7561284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535388759 |
| CDS Mutation | c.4020C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |