Colon Cancer: Gene >> TFG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100732611:100732611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519C>A
AA Mutation	p.Asn173Lys(p.N173K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100748482:100748482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373719892
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385His(p.R385H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100748475:100748475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146078119
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100720022:100720022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232A>C
AA Mutation	p.Ile78Leu(p.I78L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100713753:100713753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774808090
CDS Mutation	c.68G>A
AA Mutation	p.Arg23Gln(p.R23Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240851
Start	100748231:100748231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240851
Start	100713823:100713823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240851
Start	100713854:100713854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169A>C
AA Mutation	p.Lys57Gln(p.K57Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript