Colon Cancer: Gene >> LOXL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74536447:74536447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758787890
CDS Mutation	c.937G>A
AA Mutation	p.Ala313Thr(p.A313T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74534630:74534630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762623422
CDS Mutation	c.1724G>A
AA Mutation	p.Arg575Gln(p.R575Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74534715:74534715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639C>T
AA Mutation	p.Arg547Trp(p.R547W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74535604:74535604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400C>A
AA Mutation	p.Ala467Asp(p.A467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74535399:74535399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772977368
CDS Mutation	c.1472G>A
AA Mutation	p.Arg491His(p.R491H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74536821:74536821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800A>T
AA Mutation	p.Asp267Val(p.D267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74536303:74536303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74534105:74534105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2071C>T
AA Mutation	p.Leu691Phe(p.L691F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74536429:74536429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Trp(p.R319W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264094
Start	74535404:74535404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264094
Start	74536868:74536868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756534259
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264094
Start	74533925:74533925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2145C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264094
Start	74535714:74535714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264094
Start	74536065:74536065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264094
Start	74536797:74536797(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746133895
CDS Mutation	c.824delG
AA Mutation	p.Gly275AlafsTer5(p.G275Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000264094
Start	74552631:74552631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4C>T
AA Mutation	p.Arg2Ter(p.R2*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LOXL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74534105:74534105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2071C>A
AA Mutation	p.Leu691Ile(p.L691I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264094
Start	74552604:74552604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31C>T
AA Mutation	p.Pro11Ser(p.P11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript