Colon Cancer: Gene >> CHRNA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306901
Start	32168132:32168132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306901
Start	32157697:32157697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520G>A
AA Mutation	p.Gly174Arg(p.G174R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306901
Start	32163236:32163236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306901
Start	32168110:32168110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745942749
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000306901
Start	32158571:32158572(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.758_759insCCATAG
AA Mutation	p.Leu253_Leu254insHisArg(p.L253_L254insHR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHRNA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306901
Start	32111881:32111881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332A>G
AA Mutation	p.Asp111Gly(p.D111G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306901
Start	32158493:32158493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138222088
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript