Colon Cancer: Gene >> TNFSF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6669985:6669985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Trp(p.R29W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6665144:6665144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746091221
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6669960:6669960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110G>A
AA Mutation	p.Arg37Gln(p.R37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6669972:6669972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98G>A
AA Mutation	p.Cys33Tyr(p.C33Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6664982:6664982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772753769
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Cys(p.R223C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6665047:6665047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602G>A
AA Mutation	p.Ser201Asn(p.S201N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599359
Start	6665244:6665244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599359
Start	6669998:6669998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599359
Start	6670004:6670004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599359
Start	6667135:6667135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000599359
Start	6669993:6669993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150431195
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000599359
Start	6664985:6664985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.664delG
AA Mutation	p.Glu222AsnfsTer31(p.E222Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000599359
Start	6664973:6664973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Ter(p.R226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript