Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SERPINB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335686
Start	2948934:2948934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769858532
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335686
Start	2955652:2955652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184A>G
AA Mutation	p.Ser62Gly(p.S62G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335686
Start	2948478:2948478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335686
Start	2948334:2948334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145397970
CDS Mutation	c.1095C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000335686
Start	2948700:2948700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335686
Start	2948483:2948483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550855004
CDS Mutation	c.946G>A
AA Mutation	p.Val316Met(p.V316M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335686
Start	2954646:2954646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368785463
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335686
Start	2955650:2955650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186T>G
AA Mutation	p.Ser62Arg(p.S62R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335686
Start	2948625:2948625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804A>G
Mutation Classification	Silent
Feature Type	Transcript