Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FGD4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32638788:32638788(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2036C>T
AA Mutation p.Ala679Val(p.A679V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32598533:32598533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.637G>A
AA Mutation p.Glu213Lys(p.E213K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32633601:32633601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1814G>A
AA Mutation p.Gly605Asp(p.G605D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32633679:32633679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1892G>T
AA Mutation p.Gly631Val(p.G631V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32582037:32582037(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.170G>C
AA Mutation p.Gly57Ala(p.G57A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000427716
Start 32582242:32582242(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374075663
CDS Mutation c.375G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000427716
Start 32640470:32640470(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2238T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000427716
Start 32582071:32582071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.204C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32576401:32576401(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.48delA
AA Mutation p.Lys16AsnfsTer24(p.K16Nfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32638788:32638788(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2041delC
AA Mutation p.Gln681ArgfsTer31(p.Q681Rfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32581988:32581989(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.122_123delAA
AA Mutation p.Lys41ArgfsTer10(p.K41Rfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32638720:32638720(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1971delA
AA Mutation p.Lys657AsnfsTer9(p.K657Nfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000427716
Start 32625690:32625690(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1672C>T
AA Mutation p.Arg558Ter(p.R558*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000427716
Start 32576361:32576361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4G>T
AA Mutation p.Glu2Ter(p.E2*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32598536:32598537(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.644dupT
AA Mutation p.Leu215PhefsTer4(p.L215Ffs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000427716
Start 32582036:32582037(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.169_170insAAAA
AA Mutation p.Gly57GlufsTer23(p.G57Efs*23)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FGD4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32640379:32640379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2147C>T
AA Mutation p.Ser716Phe(p.S716F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000427716
Start 32581998:32581998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.131C>A
AA Mutation p.Ala44Asp(p.A44D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000427716
Start 32640434:32640434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2202C>A
Mutation Classification Silent
Feature Type Transcript