Colon Cancer: Gene >> LOXL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98260979:98260979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605T>C
AA Mutation	p.Val202Ala(p.V202A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98263009:98263009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779922908
CDS Mutation	c.11C>T
AA Mutation	p.Ser4Phe(p.S4F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98262748:98262748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272G>T
AA Mutation	p.Gly91Val(p.G91V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98251164:98251164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101C>T
AA Mutation	p.Pro701Ser(p.P701S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98262773:98262773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Ala83Thr(p.A83T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98253599:98253599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761221673
CDS Mutation	c.1789C>T
AA Mutation	p.Arg597Cys(p.R597C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98262851:98262851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Val57Met(p.V57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98248944:98248944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2248C>T
AA Mutation	p.Arg750Cys(p.R750C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98253682:98253682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766427951
CDS Mutation	c.1706C>T
AA Mutation	p.Ala569Val(p.A569V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98258151:98258151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750133368
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98262109:98262109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382G>A
AA Mutation	p.Val128Ile(p.V128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98261097:98261097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487C>T
AA Mutation	p.Pro163Ser(p.P163S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98262959:98262959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>G
AA Mutation	p.Pro21Ala(p.P21A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260702
Start	98255716:98255716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756777475
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260702
Start	98263014:98263014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201076968
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000260702
Start	98262859:98262859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Trp54Ter(p.W54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LOXL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260702
Start	98253610:98253610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199557224
CDS Mutation	c.1778G>A
AA Mutation	p.Arg593Gln(p.R593Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript