Colon Cancer: Gene >> CAMLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297156
Start	134738753:134738753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133A>C
AA Mutation	p.Asn45His(p.N45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297156
Start	134738691:134738691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>T
AA Mutation	p.Ala24Val(p.A24V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297156
Start	134741456:134741456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751766092
CDS Mutation	c.566G>A
AA Mutation	p.Arg189Gln(p.R189Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297156
Start	134750822:134750822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765331970
CDS Mutation	c.763G>A
AA Mutation	p.Glu255Lys(p.E255K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000297156
Start	134741440:134741440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>T
AA Mutation	p.Glu184Ter(p.E184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000297156
Start	134741140:134741140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748338400
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Ter(p.R84*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CAMLG

No Mutation Annotation!