Colon Cancer: Gene >> PPP2R2B

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394409
Start	146691129:146691129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756415160
CDS Mutation	c.446G>A
AA Mutation	p.Arg149Gln(p.R149Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146878053:146878053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19A>T
AA Mutation	p.Thr7Ser(p.T7S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146600440:146600440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811C>T
AA Mutation	p.Pro271Ser(p.P271S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146701094:146701094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119C>T
AA Mutation	p.Ala40Val(p.A40V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146650654:146650654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.518C>T
AA Mutation	p.Thr173Ile(p.T173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146691208:146691208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394409
Start	146691130:146691130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Trp(p.R149W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146590015:146590015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1264C>T
AA Mutation	p.Pro422Ser(p.P422S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394409
Start	146600450:146600450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394409
Start	146650623:146650623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771068110
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394414
Start	147055697:147055697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394409
Start	146650620:146650620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394409
Start	146590089:146590089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs767808084
CDS Mutation	c.1190delG
AA Mutation	p.Gly397AlafsTer31(p.G397Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394409
Start	146592986:146592987(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1036_1037delTG
AA Mutation	p.Trp346GlufsTer26(p.W346Efs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394409
Start	146878010:146878010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62C>T
AA Mutation	p.Ala21Val(p.A21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript