Colon Cancer: Gene >> KTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612118:55612118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70T>A
AA Mutation	p.Phe24Ile(p.F24I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612119:55612119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71T>A
AA Mutation	p.Phe24Tyr(p.F24Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55627991:55627991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043C>T
AA Mutation	p.Ala348Val(p.A348V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55663958:55663958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3094C>T
AA Mutation	p.Leu1032Phe(p.L1032F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612451:55612451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776818967
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000395314
Start	55658614:55658614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2961G>T
AA Mutation	p.Gln987His(p.Q987H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612421:55612421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748916844
CDS Mutation	c.373C>T
AA Mutation	p.Leu125Phe(p.L125F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612404:55612404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356A>C
AA Mutation	p.Lys119Thr(p.K119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55656125:55656125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2885T>G
AA Mutation	p.Leu962Arg(p.L962R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55672681:55672681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3583G>A
AA Mutation	p.Glu1195Lys(p.E1195K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55612237:55612237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189A>T
AA Mutation	p.Lys63Asn(p.K63N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395314
Start	55640379:55640379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1920A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395314
Start	55612168:55612168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55670757:55670757(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3302delA
AA Mutation	p.Lys1101ArgfsTer18(p.K1101Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55667292:55667292(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3234delA
AA Mutation	p.Lys1078AsnfsTer12(p.K1078Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55659678:55659678(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2978delC
AA Mutation	p.Pro993LeufsTer6(p.P993Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55670756:55670757(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3302dupA
AA Mutation	p.Ala1102GlyfsTer15(p.A1102Gfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55659677:55659678(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2978dupC
AA Mutation	p.His994SerfsTer2(p.H994Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55630084:55630085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1208_1209insAT
AA Mutation	p.Met404Ter(p.M404*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395314
Start	55630085:55630086(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1211_1212insAAACAAT
AA Mutation	p.Met404IlefsTer12(p.M404Ifs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395314
Start	55679590:55679590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3974C>A
AA Mutation	p.Ser1325Tyr(p.S1325Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395314
Start	55616596:55616596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395314
Start	55651910:55651910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2586T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000395314
Start	55612244:55612244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196G>T
AA Mutation	p.Glu66Ter(p.E66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000395314
Start	55661521:55661521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3000-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript