Colon Cancer: Gene >> FIBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338369
Start	65888105:65888105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338369
Start	65888117:65888117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101C>T
AA Mutation	p.Ala34Val(p.A34V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338369
Start	65885130:65885130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724A>C
AA Mutation	p.Lys242Gln(p.K242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338369
Start	65887683:65887683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328A>G
AA Mutation	p.Lys110Glu(p.K110E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338369
Start	65884989:65884989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338369
Start	65884451:65884451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751544973
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338369
Start	65885606:65885606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.570delA
AA Mutation	p.Lys190AsnfsTer5(p.K190Nfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FIBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338369
Start	65885581:65885581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595T>A
AA Mutation	p.Phe199Ile(p.F199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338369
Start	65887714:65887714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369187767
CDS Mutation	c.297T>C
Mutation Classification	Silent
Feature Type	Transcript