Colon Cancer: Gene >> TNFSF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398795
Start	42606632:42606632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775440686
CDS Mutation	c.668G>A
AA Mutation	p.Arg223Gln(p.R223Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398795
Start	42606838:42606838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>A
AA Mutation	p.Glu292Lys(p.E292K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398795
Start	42600973:42600973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524T>A
AA Mutation	p.Ile175Asn(p.I175N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398795
Start	42600766:42600766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398795
Start	42606867:42606867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs9566999
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398795
Start	42606762:42606762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000398795
Start	42606640:42606640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>T
AA Mutation	p.Glu226Ter(p.E226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000398795
Start	42606631:42606631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603829
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Ter(p.R223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000398795
Start	42600882:42600882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398795
Start	42600941:42600941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398795
Start	42606600:42606600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>A
Mutation Classification	Silent
Feature Type	Transcript