Colon Cancer: Gene >> PKIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354275
Start	122717835:122717835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41G>A
AA Mutation	p.Gly14Glu(p.G14E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354275
Start	122717878:122717878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84T>G
AA Mutation	p.Asn28Lys(p.N28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354275
Start	122717871:122717871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752581156
CDS Mutation	c.77G>A
AA Mutation	p.Arg26His(p.R26H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354275
Start	122717812:122717812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354275
Start	122717834:122717834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.43delG
AA Mutation	p.Val15SerfsTer40(p.V15Sfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354275
Start	122717936:122717936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.144delA
AA Mutation	p.Lys48AsnfsTer7(p.K48Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PKIB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354275
Start	122717914:122717914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148112687
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354275
Start	122717842:122717842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript