Colon Cancer: Gene >> F12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253496
Start	177404871:177404871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573G>T
AA Mutation	p.Glu191Asp(p.E191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253496
Start	177406047:177406047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>A
AA Mutation	p.Gly44Arg(p.G44R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253496
Start	177404534:177404534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253496
Start	177404326:177404326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751800442
CDS Mutation	c.888G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000253496
Start	177405771:177405771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Ter(p.R84*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> F12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253496
Start	177406031:177406031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146T>C
AA Mutation	p.Phe49Ser(p.F49S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript