Colon Cancer: Gene >> CLYBL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99866296:99866296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Val231Ile(p.V231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99891336:99891336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>T
AA Mutation	p.Gly316Trp(p.G316W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99870953:99870953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818A>G
AA Mutation	p.His273Arg(p.H273R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99891330:99891330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940T>A
AA Mutation	p.Phe314Ile(p.F314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99864903:99864903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626C>T
AA Mutation	p.Ala209Val(p.A209V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99891382:99891382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992T>C
AA Mutation	p.Val331Ala(p.V331A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLYBL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339105
Start	99863086:99863086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534T>G
AA Mutation	p.Asn178Lys(p.N178K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript