Colon Cancer: Gene >> CDC42BPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102947747:102947747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3505C>A
AA Mutation	p.Arg1169Ser(p.R1169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102949786:102949786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3428C>T
AA Mutation	p.Ala1143Val(p.A1143V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102972040:102972040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551755307
CDS Mutation	c.1763G>A
AA Mutation	p.Arg588His(p.R588H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361246
Start	102939611:102939611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4826T>G
AA Mutation	p.Leu1609Arg(p.L1609R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102971956:102971956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1847G>T
AA Mutation	p.Arg616Leu(p.R616L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102970216:102970216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1930C>T
AA Mutation	p.Arg644Cys(p.R644C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102970215:102970215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1931G>A
AA Mutation	p.Arg644His(p.R644H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102974077:102974077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1580G>T
AA Mutation	p.Arg527Leu(p.R527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102947796:102947796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150060973
CDS Mutation	c.3456C>G
AA Mutation	p.Asp1152Glu(p.D1152E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102971952:102971952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851G>T
AA Mutation	p.Gln617His(p.Q617H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102968299:102968299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374402137
CDS Mutation	c.2300C>T
AA Mutation	p.Ala767Val(p.A767V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	103012139:103012139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>A
AA Mutation	p.Asp75Glu(p.D75E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102978162:102978162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184A>G
AA Mutation	p.His395Arg(p.H395R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102939893:102939893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4646G>T
AA Mutation	p.Arg1549Leu(p.R1549L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102944049:102944049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776462657
CDS Mutation	c.4250C>T
AA Mutation	p.Ala1417Val(p.A1417V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102980861:102980861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772636121
CDS Mutation	c.1052G>A
AA Mutation	p.Arg351Gln(p.R351Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102954245:102954245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3019G>A
AA Mutation	p.Ala1007Thr(p.A1007T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102944146:102944146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4153A>G
AA Mutation	p.Arg1385Gly(p.R1385G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102986550:102986550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761287992
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102999642:102999642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377547128
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102944054:102944054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759603636
CDS Mutation	c.4245G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102970160:102970160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102967135:102967135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2382T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102975941:102975941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757921555
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102983610:102983610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763081501
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102954237:102954237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376465925
CDS Mutation	c.3027G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361246
Start	102963129:102963129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2753delA
AA Mutation	p.Asn918ThrfsTer5(p.N918Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361246
Start	102950558:102950558(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3217delC
AA Mutation	p.Gln1073ArgfsTer38(p.Q1073Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361246
Start	102980887:102980887(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1026delT
AA Mutation	p.Phe342LeufsTer4(p.F342Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361246
Start	102980900:102980900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1013delA
AA Mutation	p.Lys338SerfsTer8(p.K338Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000361246
Start	102939831:102939831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4708C>T
AA Mutation	p.Arg1570Ter(p.R1570*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000361246
Start	102963112:102963112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2770G>T
AA Mutation	p.Glu924Ter(p.E924*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361246
Start	102963098:102963099(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2783dupT
AA Mutation	p.Leu928PhefsTer26(p.L928Ffs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDC42BPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102970243:102970243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1903G>T
AA Mutation	p.Asp635Tyr(p.D635Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361246
Start	102972007:102972007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369423884
CDS Mutation	c.1796G>A
AA Mutation	p.Arg599Gln(p.R599Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361246
Start	102975709:102975709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377142500
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript