Colon Cancer: Gene >> PPP1R3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630520:91630520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Asp121Asn(p.D121N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630451:91630451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182503852
CDS Mutation	c.430G>A
AA Mutation	p.Asp144Asn(p.D144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630781:91630781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100C>A
AA Mutation	p.Pro34Thr(p.P34T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91629966:91629966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915G>T
AA Mutation	p.Gln305His(p.Q305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630687:91630687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194A>C
AA Mutation	p.Lys65Thr(p.K65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238994
Start	91629939:91629939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630501:91630501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380A>T
AA Mutation	p.Lys127Ile(p.K127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238994
Start	91630673:91630673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208T>C
AA Mutation	p.Ser70Pro(p.S70P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript