Colon Cancer: Gene >> LPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58250446:58250446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605A>G
AA Mutation	p.Tyr202Cys(p.Y202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58249670:58249670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Thr183Met(p.T183M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58252486:58252486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771008787
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362His(p.R362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58252363:58252363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372802766
CDS Mutation	c.962G>A
AA Mutation	p.Arg321His(p.R321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58249588:58249588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>A
AA Mutation	p.Ala156Thr(p.A156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58266237:58266237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144914036
CDS Mutation	c.1604G>A
AA Mutation	p.Arg535His(p.R535H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58249150:58249150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416G>A
AA Mutation	p.Arg139His(p.R139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58254822:58254822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>A
AA Mutation	p.Ala373Thr(p.A373T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262290
Start	58267416:58267416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1761G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262290
Start	58249578:58249578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262290
Start	58267895:58267895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2040A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262290
Start	58264781:58264782(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1331dupC
AA Mutation	p.Tyr445IlefsTer6(p.Y445Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58249063:58249063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329C>A
AA Mutation	p.Pro110His(p.P110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58266236:58266236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372987674
CDS Mutation	c.1603C>T
AA Mutation	p.Arg535Cys(p.R535C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262290
Start	58264946:58264946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1491C>A
AA Mutation	p.Phe497Leu(p.F497L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262290
Start	58254840:58254840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262290
Start	58267934:58267934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149585110
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript