Colon Cancer: Gene >> PPP2R2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26362771:26362771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725T>C
AA Mutation	p.Phe242Ser(p.F242S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26354481:26354481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194C>A
AA Mutation	p.Ser65Tyr(p.S65Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26370229:26370229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160A>C
AA Mutation	p.Lys387Thr(p.K387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26362830:26362830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784T>G
AA Mutation	p.Cys262Gly(p.C262G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26366369:26366369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027T>G
AA Mutation	p.Phe343Val(p.F343V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26370319:26370319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250A>C
AA Mutation	p.Lys417Thr(p.K417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380737
Start	26360203:26360203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380737
Start	26354533:26354533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380737
Start	26361087:26361087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380737
Start	26361144:26361144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380737
Start	26363756:26363756(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.844delT
AA Mutation	p.Ser282ProfsTer10(p.S282Pfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000380737
Start	26338928:26338928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>T
AA Mutation	p.Glu41Ter(p.E41*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380737
Start	26354599:26354600(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.317dupA
AA Mutation	p.Asn106LysfsTer11(p.N106Kfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000380737
Start	26361142:26361143(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.628_629insCAT
AA Mutation	p.Arg210delinsThrTrp(p.R210delinsTW)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380737
Start	26370390:26370390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321A>G
AA Mutation	p.Ile441Val(p.I441V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380737
Start	26370215:26370215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000380737
Start	26338928:26338928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>T
AA Mutation	p.Glu41Ter(p.E41*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript