Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MYB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135185962:135185962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83G>T
AA Mutation	p.Gly28Val(p.G28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135192467:135192467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135195775:135195775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750351406
CDS Mutation	c.976G>A
AA Mutation	p.Gly326Arg(p.G326R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367814
Start	135186021:135186021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MYB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135192368:135192368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191Gln(p.R191Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135200168:135200168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1430A>G
AA Mutation	p.Gln477Arg(p.Q477R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135200129:135200129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391C>G
AA Mutation	p.Pro464Arg(p.P464R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367814
Start	135190328:135190328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367814
Start	135190327:135190327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript