Colon Cancer: Gene >> PRSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142752476:142752476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500G>A
AA Mutation	p.Ser167Asn(p.S167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142751810:142751810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>C
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142752015:142752015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142751953:142751953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>A
AA Mutation	p.Ser127Tyr(p.S127Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142752486:142752486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510G>T
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311737
Start	142752537:142752537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1804561
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311737
Start	142751989:142751990(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.418dupC
AA Mutation	p.Leu140ProfsTer31(p.L140Pfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000311737
Start	142750554:142750554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311737
Start	142752015:142752015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>T
AA Mutation	p.Ala148Ser(p.A148S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript