Colon Cancer: Gene >> LFNG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222725
Start	2525493:2525493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377387325
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Trp(p.R221W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222725
Start	2525257:2525257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373426024
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222725
Start	2525536:2525536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704A>C
AA Mutation	p.Gln235Pro(p.Q235P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222725
Start	2525502:2525502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670T>C
AA Mutation	p.Tyr224His(p.Y224H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222725
Start	2525282:2525282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Ala182Val(p.A182V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402506
Start	2513169:2513169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402506
Start	2513194:2513194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222725
Start	2525714:2525714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201724400
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LFNG

No Mutation Annotation!