Colon Cancer: Gene >> PIK3C2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204439002:204439002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3449C>T
AA Mutation	p.Ser1150Leu(p.S1150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204460599:204460599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61755372
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458Gln(p.R458Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204443442:204443442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114563071
CDS Mutation	c.3023G>A
AA Mutation	p.Arg1008Gln(p.R1008Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204460621:204460621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351C>A
AA Mutation	p.Arg451Ser(p.R451S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204447494:204447494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431C>T
AA Mutation	p.Leu811Phe(p.L811F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204442549:204442549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3133C>A
AA Mutation	p.Leu1045Met(p.L1045M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204457750:204457750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770614232
CDS Mutation	c.1691G>A
AA Mutation	p.Arg564His(p.R564H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204433392:204433392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3877C>A
AA Mutation	p.Leu1293Met(p.L1293M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204464036:204464036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Cys429Tyr(p.C429Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204447511:204447511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780535663
CDS Mutation	c.2414G>A
AA Mutation	p.Arg805His(p.R805H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204469180:204469180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623T>C
AA Mutation	p.Leu208Pro(p.L208P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204460605:204460605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367A>G
AA Mutation	p.Asp456Gly(p.D456G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204433912:204433912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3724T>C
AA Mutation	p.Tyr1242His(p.Y1242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204440233:204440233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368018698
CDS Mutation	c.3338G>A
AA Mutation	p.Arg1113His(p.R1113H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204469721:204469721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>A
AA Mutation	p.Glu28Lys(p.E28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204433880:204433880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3756C>A
AA Mutation	p.Ser1252Arg(p.S1252R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204442594:204442594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3088T>G
AA Mutation	p.Phe1030Val(p.F1030V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204460621:204460621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773548781
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Cys(p.R451C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367187
Start	204446009:204446009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2625G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367187
Start	204424945:204424945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61758019
CDS Mutation	c.4812C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367187
Start	204443450:204443450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3015G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367187
Start	204457761:204457761(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1680delC
AA Mutation	p.Cys561AlafsTer18(p.C561Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000367187
Start	204454678:204454678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2057G>A
AA Mutation	p.Trp686Ter(p.W686*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367187
Start	204468943:204468944(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749506841
CDS Mutation	c.859dupC
AA Mutation	p.Arg287ProfsTer38(p.R287Pfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3C2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204443491:204443491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974C>T
AA Mutation	p.Arg992Cys(p.R992C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204432285:204432285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779751747
CDS Mutation	c.4070G>A
AA Mutation	p.Arg1357Gln(p.R1357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367187
Start	204464599:204464599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2271416
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367187
Start	204424885:204424885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577562908
CDS Mutation	c.4872C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367187
Start	204449937:204449937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2147delC
AA Mutation	p.Pro716HisfsTer32(p.P716Hfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript