Colon Cancer: Gene >> PNOC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301908
Start	28339416:28339416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763003120
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301908
Start	28329233:28329233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76C>G
AA Mutation	p.Leu26Val(p.L26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301908
Start	28339140:28339140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780712455
CDS Mutation	c.227C>T
AA Mutation	p.Ala76Val(p.A76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301908
Start	28339182:28339182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764588634
CDS Mutation	c.269C>T
AA Mutation	p.Ser90Leu(p.S90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301908
Start	28339156:28339156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PNOC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301908
Start	28329192:28329192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35G>A
AA Mutation	p.Ser12Asn(p.S12N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript