Colon Cancer: Gene >> LOXL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23303375:23303375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1903T>A
AA Mutation	p.Phe635Ile(p.F635I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23360106:23360106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515T>G
AA Mutation	p.Leu172Trp(p.L172W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23317015:23317015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570G>A
AA Mutation	p.Asp524Asn(p.D524N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23341149:23341149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143674437
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23309852:23309852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766054276
CDS Mutation	c.1696C>T
AA Mutation	p.Arg566Trp(p.R566W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23333411:23333411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956A>G
AA Mutation	p.Tyr319Cys(p.Y319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23309768:23309768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Cys(p.R594C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23341041:23341041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751602145
CDS Mutation	c.694G>A
AA Mutation	p.Gly232Ser(p.G232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23368141:23368141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763353774
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23368192:23368192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23302092:23302092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755780161
CDS Mutation	c.2068C>T
AA Mutation	p.Arg690Cys(p.R690C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23322211:23322211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>A
AA Mutation	p.Phe407Leu(p.F407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23333598:23333598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756691275
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Cys(p.R257C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23319977:23319977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378T>G
AA Mutation	p.Trp460Gly(p.W460G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389131
Start	23360189:23360189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389131
Start	23309727:23309727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1821C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389131
Start	23328476:23328476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389131
Start	23317097:23317097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374553547
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389131
Start	23298092:23298092(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2276delA
AA Mutation	p.Lys759SerfsTer9(p.K759Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000389131
Start	23341170:23341170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759081095
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Ter(p.R189*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LOXL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23360169:23360169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186026557
CDS Mutation	c.452C>T
AA Mutation	p.Thr151Met(p.T151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389131
Start	23341085:23341085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650T>G
AA Mutation	p.Ile217Ser(p.I217S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389131
Start	23322277:23322277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199848147
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript