Colon Cancer: Gene >> FGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302068
Start	154569641:154569641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086G>T
AA Mutation	p.Gln362His(p.Q362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302068
Start	154569765:154569765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210T>C
AA Mutation	p.Phe404Leu(p.F404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302068
Start	154570504:154570504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>A
AA Mutation	p.Gly444Ser(p.G444S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302068
Start	154570644:154570644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302068
Start	154565885:154565885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761354866
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302068
Start	154567697:154567697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747314723
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302068
Start	154567688:154567688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909623
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript