Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17607503:17607503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474G>A
AA Mutation	p.Val492Ile(p.V492I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17597106:17597106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1049T>C
AA Mutation	p.Val350Ala(p.V350A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17579851:17579851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>A
AA Mutation	p.Glu44Lys(p.E44K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17588883:17588883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748906411
CDS Mutation	c.769G>A
AA Mutation	p.Glu257Lys(p.E257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17588890:17588890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>A
AA Mutation	p.Pro259Gln(p.P259Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17577544:17577544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79C>T
AA Mutation	p.Leu27Phe(p.L27F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226299
Start	17583532:17583532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17581792:17581792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781094926
CDS Mutation	c.251G>A
AA Mutation	p.Arg84Gln(p.R84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226299
Start	17607566:17607566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537C>T
AA Mutation	p.Arg513Cys(p.R513C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226299
Start	17607442:17607442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749403844
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226299
Start	17598527:17598527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147122901
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000226299
Start	17582369:17582369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>T
AA Mutation	p.Glu119Ter(p.E119*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript