Colon Cancer: Gene >> PPP1R42

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67017647:67017647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101A>T
AA Mutation	p.Asn34Ile(p.N34I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67017706:67017706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42T>A
AA Mutation	p.Asn14Lys(p.N14K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67012965:67012965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>A
AA Mutation	p.Ser143Tyr(p.S143Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67014586:67014586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>T
AA Mutation	p.Leu46Phe(p.L46F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R42

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67010806:67010806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>A
AA Mutation	p.Ser154Asn(p.S154N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324682
Start	67017662:67017662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774838939
CDS Mutation	c.86A>C
AA Mutation	p.Lys29Thr(p.K29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript