Primary Site >> Stomach Cancer
Gene >> FRMD6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51720360:51720360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1330G>A |
| AA Mutation | p.Asp444Asn(p.D444N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51720124:51720124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542106517 |
| CDS Mutation | c.1094G>T |
| AA Mutation | p.Arg365Leu(p.R365L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51708159:51708159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563838195 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Glu214Lys(p.E214K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51720148:51720148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371612348 |
| CDS Mutation | c.1118C>T |
| AA Mutation | p.Ala373Val(p.A373V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51708115:51708115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596A>G |
| AA Mutation | p.His199Arg(p.H199R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000344768 |
| Start | 51712549:51712549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.847G>A |
| AA Mutation | p.Val283Met(p.V283M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51704908:51704908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.531C>A |
| AA Mutation | p.Phe177Leu(p.F177L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51722059:51722059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748860055 |
| CDS Mutation | c.1471C>T |
| AA Mutation | p.Arg491Trp(p.R491W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344768 |
| Start | 51708207:51708207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374236968 |
| CDS Mutation | c.688G>A |
| AA Mutation | p.Ala230Thr(p.A230T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344768 |
| Start | 51711554:51711554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769310184 |
| CDS Mutation | c.738G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |