Colon Cancer: Gene >> TYMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50529314:50529314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239T>G
AA Mutation	p.Leu80Arg(p.L80R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50529170:50529170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383T>A
AA Mutation	p.Val128Asp(p.V128D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50528602:50528602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426G>A
AA Mutation	p.Met142Ile(p.M142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50529323:50529323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230C>T
AA Mutation	p.Ala77Val(p.A77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50529304:50529304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249G>T
AA Mutation	p.Met83Ile(p.M83I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252029
Start	50527653:50527653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Ala194Val(p.A194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252029
Start	50525881:50525881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252029
Start	50527216:50527216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252029
Start	50527262:50527263(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.667_668insCCGTGGAGGGGCTGAGAATGGAGGCATTCTCAGTAAGAAAC
AA Mutation	p.Leu223ProfsTer54(p.L223Pfs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TYMP

No Mutation Annotation!