Colon Cancer: Gene >> PPP2R1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52213076:52213076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258His(p.R258H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52212729:52212729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Trp(p.R183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52212735:52212735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Ala185Thr(p.A185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52211401:52211401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Gly138Ser(p.G138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52211333:52211333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>C
AA Mutation	p.Ile115Thr(p.I115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52216610:52216610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075G>A
AA Mutation	p.Asp359Asn(p.D359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52216590:52216590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055T>C
AA Mutation	p.Leu352Pro(p.L352P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52212969:52212969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52222221:52222221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1641A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52219747:52219747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52212975:52212975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52211301:52211301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000322088
Start	52222242:52222242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1661+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52212828:52212828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Glu216Lys(p.E216K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322088
Start	52220200:52220200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314C>A
AA Mutation	p.Phe438Leu(p.F438L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322088
Start	52201949:52201949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript