Colon Cancer: Gene >> KIF18A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28036610:28036610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372157089
CDS Mutation	c.2003G>A
AA Mutation	p.Arg668Gln(p.R668Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28097899:28097899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28097916:28097916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763203090
CDS Mutation	c.32A>G
AA Mutation	p.His11Arg(p.H11R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28077134:28077134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200731334
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433Gln(p.R433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28035439:28035439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2452C>T
AA Mutation	p.Pro818Ser(p.P818S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28023798:28023798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2557C>T
AA Mutation	p.Arg853Cys(p.R853C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28069303:28069303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374462377
CDS Mutation	c.1546G>A
AA Mutation	p.Glu516Lys(p.E516K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28088568:28088568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>A
AA Mutation	p.Leu285Ile(p.L285I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28059150:28059150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756594556
CDS Mutation	c.1724C>T
AA Mutation	p.Ala575Val(p.A575V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28035400:28035400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142577501
CDS Mutation	c.2491C>T
AA Mutation	p.Arg831Trp(p.R831W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28084689:28084689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28036591:28036591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2022T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28036371:28036371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28069304:28069304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28036453:28036453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2160A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263181
Start	28097708:28097708(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.240delT
AA Mutation	p.Phe80LeufsTer23(p.F80Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263181
Start	28091442:28091442(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.555delA
AA Mutation	p.Val187TrpfsTer35(p.V187Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263181
Start	28036616:28036617(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1996dupA
AA Mutation	p.Arg666LysfsTer29(p.R666Kfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF18A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263181
Start	28097899:28097899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263181
Start	28082861:28082861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370457263
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263181
Start	28097708:28097708(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.240delT
AA Mutation	p.Phe80LeufsTer23(p.F80Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript