Colon Cancer: Gene >> LTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28986816:28986816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28967073:28967073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752825301
CDS Mutation	c.1418C>T
AA Mutation	p.Thr473Met(p.T473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28986768:28986768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209G>A
AA Mutation	p.Arg70Gln(p.R70Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28959589:28959589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2462C>T
AA Mutation	p.Ser821Phe(p.S821F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28945916:28945916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3659T>C
AA Mutation	p.Val1220Ala(p.V1220A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28966402:28966402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2089G>A
AA Mutation	p.Glu697Lys(p.E697K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361371
Start	28935145:28935145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4839T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361371
Start	28946223:28946223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361371
Start	28960656:28960656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183572524
CDS Mutation	c.2214C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361371
Start	28931296:28931296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5097T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28966524:28966524(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1967delA
AA Mutation	p.Asn656IlefsTer11(p.N656Ifs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28969538:28969538(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1239delT
AA Mutation	p.Phe413LeufsTer7(p.F413Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28959470:28959470(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2581delA
AA Mutation	p.Thr861HisfsTer11(p.T861Hfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000361371
Start	28944440:28944440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3925G>T
AA Mutation	p.Glu1309Ter(p.E1309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000361371
Start	28959476:28959476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575G>T
AA Mutation	p.Glu859Ter(p.E859*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000361371
Start	28966672:28966672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1819G>T
AA Mutation	p.Glu607Ter(p.E607*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000361371
Start	28946249:28946249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3526C>T
AA Mutation	p.Gln1176Ter(p.Q1176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28941327:28941328(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4374_4375insA
AA Mutation	p.Gly1459ArgfsTer7(p.G1459Rfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28941329:28941330(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4372_4373insAAGCATA
AA Mutation	p.Val1458GlufsTer10(p.V1458Efs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361371
Start	28960696:28960697(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2173_2174insTTTTTAACAT
AA Mutation	p.Ser725IlefsTer7(p.S725Ifs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361371
Start	28953377:28953377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3080-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28952169:28952169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3335G>A
AA Mutation	p.Arg1112Lys(p.R1112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28971382:28971382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873A>C
AA Mutation	p.Lys291Asn(p.K291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28981158:28981158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771G>T
AA Mutation	p.Gln257His(p.Q257H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28992783:28992783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23G>C
AA Mutation	p.Arg8Pro(p.R8P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28945914:28945914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3661A>C
AA Mutation	p.Asn1221His(p.N1221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28960569:28960569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2301C>A
AA Mutation	p.Phe767Leu(p.F767L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28969528:28969528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369131368
CDS Mutation	c.1249C>T
AA Mutation	p.Arg417Cys(p.R417C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28953331:28953331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3125A>G
AA Mutation	p.Asn1042Ser(p.N1042S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361371
Start	28971303:28971303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>A
AA Mutation	p.Glu318Lys(p.E318K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361371
Start	28953354:28953354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3102G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361371
Start	28981300:28981300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript