Colon Cancer: Gene >> CPA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222482
Start	130293240:130293240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60A>C
AA Mutation	p.Lys20Asn(p.K20N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222482
Start	130304559:130304559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367921847
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Trp(p.R156W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222482
Start	130312048:130312048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368498370
CDS Mutation	c.1004C>T
AA Mutation	p.Ala335Val(p.A335V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222482
Start	130310815:130310815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147861630
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222482
Start	130308327:130308327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000222482
Start	130308317:130308317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713G>A
AA Mutation	p.Trp238Ter(p.W238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion;splice_region_variant
Transcription ID	ENST00000222482
Start	130304579:130304580(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.486_486+1insCATGAAAGA
AA Mutation	p.Lys162_Phe163insHisGluArg(p.K162_F163insHER)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CPA4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222482
Start	130322511:130322511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778346915
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript