Colon Cancer: Gene >> LYPD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244333
Start	43461476:43461476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779677919
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244333
Start	43461751:43461751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641C>A
AA Mutation	p.Ser214Tyr(p.S214Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244333
Start	43465496:43465496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76G>A
AA Mutation	p.Gly26Arg(p.G26R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244333
Start	43464399:43464399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137C>T
AA Mutation	p.Pro46Leu(p.P46L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244333
Start	43461492:43461492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767100969
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244333
Start	43465511:43465511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LYPD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244333
Start	43463198:43463198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472G>A
AA Mutation	p.Val158Ile(p.V158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244333
Start	43461495:43461495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202091507
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript