Primary Site >> Stomach Cancer

Gene >> FER

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000281092
Start 109100517:109100517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2046C>G
AA Mutation p.His682Gln(p.H682Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 109186296:109186296(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2300A>G
AA Mutation p.Gln767Arg(p.Q767R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 108897739:108897739(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1127A>G
AA Mutation p.Lys376Arg(p.K376R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 108959244:108959244(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1553G>A
AA Mutation p.Gly518Asp(p.G518D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 109187489:109187489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2383A>G
AA Mutation p.Lys795Glu(p.K795E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 108959304:108959304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1613T>C
AA Mutation p.Ile538Thr(p.I538T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 109044762:109044762(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1796A>G
AA Mutation p.Gln599Arg(p.Q599R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000281092
Start 108871369:108871369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.670G>T
AA Mutation p.Gly224Cys(p.G224C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000281092
Start 108954875:108954875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1476T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000281092
Start 108959329:108959329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1638G>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000281092
Start 108959330:108959330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1639C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000281092
Start 109187506:109187506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2400A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000281092
Start 108954821:108954821(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1428delA
AA Mutation p.Lys476AsnfsTer53(p.K476Nfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000281092
Start 108883400:108883400(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.931delA
AA Mutation p.Thr311ArgfsTer2(p.T311Rfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000281092
Start 108832917:108832917(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355C>T
AA Mutation p.Gln119Ter(p.Q119*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000281092
Start 108959234:108959234(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1543C>T
AA Mutation p.Arg515Ter(p.R515*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000281092
Start 108867934:108867934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.649G>T
AA Mutation p.Glu217Ter(p.E217*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000281092
Start 108798319:108798319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137T>A
AA Mutation p.Leu46Ter(p.L46*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript