Primary Site >> Esophagus Cancer
Gene >> FLG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310802:152310802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4084C>G |
| AA Mutation | p.Gln1362Glu(p.Q1362E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309944:152309944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4942G>C |
| AA Mutation | p.Glu1648Gln(p.E1648Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308914:152308914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556604607 |
| CDS Mutation | c.5972C>T |
| AA Mutation | p.Ala1991Val(p.A1991V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308030:152308030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770039879 |
| CDS Mutation | c.6856C>T |
| AA Mutation | p.His2286Tyr(p.H2286Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311243:152311243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3643A>C |
| AA Mutation | p.Ser1215Arg(p.S1215R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311617:152311617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3269G>A |
| AA Mutation | p.Gly1090Glu(p.G1090E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312478:152312478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2408C>A |
| AA Mutation | p.Ser803Tyr(p.S803Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308870:152308870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6016G>A |
| AA Mutation | p.Gly2006Arg(p.G2006R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305408:152305408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9478A>G |
| AA Mutation | p.Ser3160Gly(p.S3160G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306151:152306151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8735C>G |
| AA Mutation | p.Ser2912Cys(p.S2912C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306503:152306503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779385755 |
| CDS Mutation | c.8383G>A |
| AA Mutation | p.Gly2795Arg(p.G2795R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308926:152308926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150720370 |
| CDS Mutation | c.5960G>A |
| AA Mutation | p.Arg1987His(p.R1987H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313190:152313190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696A>C |
| AA Mutation | p.Ser566Arg(p.S566R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307459:152307459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780111314 |
| CDS Mutation | c.7427C>A |
| AA Mutation | p.Ser2476Tyr(p.S2476Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304373:152304373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10513C>T |
| AA Mutation | p.His3505Tyr(p.H3505Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304304:152304304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10582G>A |
| AA Mutation | p.Gly3528Arg(p.G3528R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308459:152308459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6427G>A |
| AA Mutation | p.Gly2143Arg(p.G2143R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308320:152308320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6566C>A |
| AA Mutation | p.Ala2189Glu(p.A2189E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152308324:152308324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6562A>G |
| AA Mutation | p.Ser2188Gly(p.S2188G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313402:152313402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139321371 |
| CDS Mutation | c.1484C>T |
| AA Mutation | p.Ser495Leu(p.S495L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314275:152314275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.611T>G |
| AA Mutation | p.Leu204Arg(p.L204R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311263:152311263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201515356 |
| CDS Mutation | c.3623A>G |
| AA Mutation | p.His1208Arg(p.H1208R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311435:152311435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3451G>A |
| AA Mutation | p.Asp1151Asn(p.D1151N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309790:152309790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778016068 |
| CDS Mutation | c.5096G>A |
| AA Mutation | p.Arg1699His(p.R1699H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309442:152309442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5444G>A |
| AA Mutation | p.Gly1815Glu(p.G1815E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152311716:152311716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3170C>A |
| AA Mutation | p.Ala1057Glu(p.A1057E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310271:152310271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536230632 |
| CDS Mutation | c.4615A>C |
| AA Mutation | p.Ser1539Arg(p.S1539R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305191:152305191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9695C>T |
| AA Mutation | p.Ser3232Phe(p.S3232F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304929:152304929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774241945 |
| CDS Mutation | c.9957G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310875:152310875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4011C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152312117:152312117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757865005 |
| CDS Mutation | c.2769T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309390:152309390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187802033 |
| CDS Mutation | c.5496G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309279:152309279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5607T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152305710:152305710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9176C>A |
| AA Mutation | p.Ser3059Ter(p.S3059*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152308543:152308543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6343C>T |
| AA Mutation | p.Gln2115Ter(p.Q2115*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152304837:152304837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10049C>G |
| AA Mutation | p.Ser3350Ter(p.S3350*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314668:152314669(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.213_217dupCACTG |
| AA Mutation | p.Glu73AlafsTer6(p.E73Afs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |