Colon Cancer: Gene >> RCAN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330430
Start	46248857:46248857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Val43Met(p.V43M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330430
Start	46248826:46248826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158G>A
AA Mutation	p.Arg53His(p.R53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330430
Start	46325451:46325451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29T>C
AA Mutation	p.Val10Ala(p.V10A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330430
Start	46223173:46223173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770255594
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Cys(p.R188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000371374
Start	46456847:46456847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>T
AA Mutation	p.Glu44Ter(p.E44*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000330430
Start	46325392:46325392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371374
Start	46456897:46456899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.78_80delCTT
AA Mutation	p.Phe26del(p.F26del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RCAN2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000330430
Start	46248788:46248788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Ter(p.R66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript