Colon Cancer: Gene >> FASLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367721
Start	172665841:172665841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671T>G
AA Mutation	p.Met224Arg(p.M224R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367721
Start	172665889:172665889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719C>T
AA Mutation	p.Ala240Val(p.A240V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367721
Start	172659381:172659381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753980291
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367721
Start	172659378:172659378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559795993
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367721
Start	172664355:172664355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs35774809
CDS Mutation	c.422delA
AA Mutation	p.Lys141ArgfsTer3(p.K141Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FASLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367721
Start	172659401:172659401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200C>T
AA Mutation	p.Pro67Leu(p.P67L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript