Primary Site >> Stomach Cancer
Gene >> FOXG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768099:28768099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.820C>T |
| AA Mutation | p.Arg274Trp(p.R274W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768274:28768274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.995C>T |
| AA Mutation | p.Ser332Leu(p.S332L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768091:28768091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs796052469 |
| CDS Mutation | c.812G>A |
| AA Mutation | p.Gly271Asp(p.G271D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768127:28768127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848A>G |
| AA Mutation | p.Lys283Arg(p.K283R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768102:28768102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.823C>T |
| AA Mutation | p.Arg275Cys(p.R275C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768007:28768007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.728C>T |
| AA Mutation | p.Pro243Leu(p.P243L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767850:28767850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.571A>G |
| AA Mutation | p.Met191Val(p.M191V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767991:28767991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712T>A |
| AA Mutation | p.Cys238Ser(p.C238S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767911:28767911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632T>C |
| AA Mutation | p.Ile211Thr(p.I211T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768399:28768399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1120T>C |
| AA Mutation | p.Tyr374His(p.Y374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28767967:28767967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.688C>G |
| AA Mutation | p.Arg230Gly(p.R230G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768111:28768111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.832A>G |
| AA Mutation | p.Thr278Ala(p.T278A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768087:28768087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.808A>C |
| AA Mutation | p.Thr270Pro(p.T270P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768049:28768049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.770T>C |
| AA Mutation | p.Leu257Pro(p.L257P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768185:28768185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768551:28768551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757300535 |
| CDS Mutation | c.1272G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768608:28768608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1329G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768434:28768434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768386:28768386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747996412 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768263:28768263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774246700 |
| CDS Mutation | c.984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313071 |
| Start | 28768684:28768684(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1409delG |
| AA Mutation | p.Gly470AspfsTer18(p.G470Dfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |