Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TAPBPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6453708:6453708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758936057
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6453528:6453528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774541786
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6453504:6453504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353A>C
AA Mutation	p.Lys118Thr(p.K118T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6458818:6458818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266556
Start	6453643:6453643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266556
Start	6453511:6453511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAPBPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6457665:6457665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825A>G
AA Mutation	p.Ile275Met(p.I275M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6458756:6458756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016A>G
AA Mutation	p.Glu339Gly(p.E339G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266556
Start	6453708:6453708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758936057
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript