Colon Cancer: Gene >> LAG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6778347:6778347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535C>T
AA Mutation	p.Pro512Leu(p.P512L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6775393:6775393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902C>A
AA Mutation	p.Pro301His(p.P301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6777341:6777341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141308793
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Cys(p.R379C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000203629
Start	6772908:6772908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56C>T
AA Mutation	p.Pro19Leu(p.P19L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6773252:6773252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119C>T
AA Mutation	p.Ala40Val(p.A40V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6772884:6772884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32T>G
AA Mutation	p.Phe11Cys(p.F11C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000203629
Start	6777442:6777442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000203629
Start	6774711:6774711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Ter(p.R210*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000203629
Start	6774594:6774594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LAG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203629
Start	6775338:6775338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript