Colon Cancer: Gene >> FBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94593681:94593681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766630515
CDS Mutation	c.46C>T
AA Mutation	p.Arg16Cys(p.R16C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94567351:94567351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624G>T
AA Mutation	p.Lys208Asn(p.K208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94559129:94559129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547312807
CDS Mutation	c.829C>T
AA Mutation	p.Arg277Trp(p.R277W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94563430:94563430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737T>C
AA Mutation	p.Val246Ala(p.V246A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94571599:94571599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430T>C
AA Mutation	p.Ser144Pro(p.S144P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375337
Start	94563426:94563426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375337
Start	94571591:94571591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375337
Start	94593676:94593676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774531216
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375337
Start	94587445:94587445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369230549
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000375337
Start	94558961:94558961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>T
AA Mutation	p.Gln333Ter(p.Q333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94571526:94571526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503A>G
AA Mutation	p.Tyr168Cys(p.Y168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375337
Start	94571556:94571556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751410821
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript