Colon Cancer: Gene >> PIK3CB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138656270:138656270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138462760
CDS Mutation	c.2947C>T
AA Mutation	p.Arg983Cys(p.R983C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138759288:138759288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148660928
CDS Mutation	c.56C>T
AA Mutation	p.Ala19Val(p.A19V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138755862:138755862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289C>G
AA Mutation	p.Arg97Gly(p.R97G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138655393:138655393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3209C>A
AA Mutation	p.Ser1070Tyr(p.S1070Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138759262:138759262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Gly28Ser(p.G28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138665092:138665092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2616T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138714690:138714690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138714519:138714519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543449352
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289153
Start	138663914:138663914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2788delA
AA Mutation	p.Thr930LeufsTer62(p.T930Lfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000289153
Start	138665049:138665049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2659G>T
AA Mutation	p.Glu887Ter(p.E887*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000289153
Start	138704449:138704451(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1573_1575delAAT
AA Mutation	p.Asn525del(p.N525del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3CB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138734644:138734644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Gln(p.R321Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138759207:138759207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137T>A
AA Mutation	p.Val46Glu(p.V46E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289153
Start	138742611:138742611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>T
AA Mutation	p.Asp190Tyr(p.D190Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289153
Start	138684777:138684777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2163T>G
Mutation Classification	Silent
Feature Type	Transcript