Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXK2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000335255
Start 82563518:82563518(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.584G>A
AA Mutation p.Ser195Asn(p.S195N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000335255
Start 82582922:82582922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1091C>T
AA Mutation p.Pro364Leu(p.P364L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000335255
Start 82582771:82582771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.940C>T
AA Mutation p.Arg314Cys(p.R314C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82585935:82585935(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1311C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82563435:82563435(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148118470
CDS Mutation c.501G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82582821:82582821(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762735443
CDS Mutation c.990G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82587250:82587250(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145491566
CDS Mutation c.1764G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82563501:82563501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.567C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000335255
Start 82586097:82586097(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748655226
CDS Mutation c.1473G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000335255
Start 82582740:82582740(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.910-1G>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> FOXK2

No Mutation Annotation!