Primary Site >> Stomach Cancer
Gene >> TTF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132392200:132392200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1863C>G |
| AA Mutation | p.Ser621Arg(p.S621R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402695:132402695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127G>T |
| AA Mutation | p.Val43Leu(p.V43L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402188:132402188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Ala212Thr(p.A212T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132376043:132376043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2590G>A |
| AA Mutation | p.Asp864Asn(p.D864N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132400195:132400195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1431A>T |
| AA Mutation | p.Leu477Phe(p.L477F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132390647:132390647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2172A>C |
| AA Mutation | p.Glu724Asp(p.E724D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132401641:132401641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1181T>G |
| AA Mutation | p.Leu394Arg(p.L394R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402238:132402238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584A>G |
| AA Mutation | p.Glu195Gly(p.E195G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334270 |
| Start | 132400160:132400160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757835009 |
| CDS Mutation | c.1466C>T |
| AA Mutation | p.Ala489Val(p.A489V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132376023:132376023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201618724 |
| CDS Mutation | c.2610C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402102:132402102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143824332 |
| CDS Mutation | c.720G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132376161:132376161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2472C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402720:132402720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.102C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132392140:132392140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1923G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334270 |
| Start | 132401763:132401763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759510256 |
| CDS Mutation | c.1059C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334270 |
| Start | 132401815:132401815(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1007delA |
| AA Mutation | p.Lys336ArgfsTer87(p.K336Rfs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334270 |
| Start | 132402001:132402001(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs770528448 |
| CDS Mutation | c.821delA |
| AA Mutation | p.Lys274SerfsTer149(p.K274Sfs*149) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334270 |
| Start | 132401986:132401986(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.836delA |
| AA Mutation | p.Lys279ArgfsTer144(p.K279Rfs*144) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000334270 |
| Start | 132401621:132401621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769896687 |
| CDS Mutation | c.1201C>T |
| AA Mutation | p.Arg401Ter(p.R401*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334270 |
| Start | 132401814:132401815(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772401251 |
| CDS Mutation | c.1007dupA |
| AA Mutation | p.Lys337GlufsTer9(p.K337Efs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |