Colon Cancer: Gene >> TGFB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41348443:41348443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368A>T
AA Mutation	p.Lys123Met(p.K123M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41348369:41348369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142642007
CDS Mutation	c.442G>A
AA Mutation	p.Val148Met(p.V148M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41331126:41331126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>A
AA Mutation	p.Val367Met(p.V367M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41342016:41342016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727C>A
AA Mutation	p.Arg243Ser(p.R243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41341914:41341914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829C>T
AA Mutation	p.Arg277Cys(p.R277C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41344828:41344828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201055697
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Trp(p.R185W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221930
Start	41348415:41348415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199696548
CDS Mutation	c.396T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000221930
Start	41332212:41332212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930G>A
AA Mutation	p.Trp310Ter(p.W310*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TGFB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221930
Start	41332259:41332259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883G>A
AA Mutation	p.Val295Met(p.V295M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript