Colon Cancer: Gene >> TNFRSF11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118924669:118924669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911G>T
AA Mutation	p.Gly304Val(p.G304V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118933050:118933050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>C
AA Mutation	p.Lys94Thr(p.K94T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118933000:118933000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201167408
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118926611:118926611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201393730
CDS Mutation	c.700G>A
AA Mutation	p.Ala234Thr(p.A234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118924583:118924583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>G
AA Mutation	p.Arg333Gly(p.R333G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297350
Start	118933145:118933145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142201380
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297350
Start	118924575:118924575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000297350
Start	118933045:118933045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>T
AA Mutation	p.Glu96Ter(p.E96*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000297350
Start	118924583:118924583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Ter(p.R333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000297350
Start	118933109:118933109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222G>A
AA Mutation	p.Trp74Ter(p.W74*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118924694:118924694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145316984
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Cys(p.R296C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297350
Start	118933036:118933036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295C>A
AA Mutation	p.Arg99Ser(p.R99S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript