Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PDCD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110881526:110881526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.Pro113Ser(p.P113S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110881497:110881497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110885309:110885309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>T
AA Mutation	p.Lys166Asn(p.K166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110881387:110881387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198C>G
AA Mutation	p.Asn66Lys(p.N66K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110885344:110885344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533A>G
AA Mutation	p.His178Arg(p.H178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280154
Start	110881385:110881386(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.196_197insGAGAG
AA Mutation	p.Asn66ArgfsTer26(p.N66Rfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000280154
Start	110895947:110895947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PDCD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110881343:110881343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754525539
CDS Mutation	c.154G>A
AA Mutation	p.Glu52Lys(p.E52K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110896071:110896071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1333G>T
AA Mutation	p.Asp445Tyr(p.D445Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280154
Start	110887845:110887845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>T
AA Mutation	p.Asp246Tyr(p.D246Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280154
Start	110898040:110898040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280154
Start	110894171:110894171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185605824
CDS Mutation	c.1071T>G
Mutation Classification	Silent
Feature Type	Transcript