Colon Cancer: Gene >> TNFRSF11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62369440:62369440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523G>T
AA Mutation	p.Gly508Val(p.G508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62354408:62354408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Val101Met(p.V101M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62359992:62359992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>G
AA Mutation	p.Thr187Ala(p.T187A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62359978:62359978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545T>C
AA Mutation	p.Val182Ala(p.V182A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62368737:62368737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745367315
CDS Mutation	c.820G>A
AA Mutation	p.Ala274Thr(p.A274T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62348180:62348180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88A>C
AA Mutation	p.Ile30Leu(p.I30L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586569
Start	62384767:62384767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586569
Start	62366736:62366736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586569
Start	62359982:62359982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000586569
Start	62366718:62366718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741G>A
AA Mutation	p.Trp247Ter(p.W247*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586569
Start	62349827:62349827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173C>A
AA Mutation	p.Ser58Tyr(p.S58Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586569
Start	62348224:62348224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000586569
Start	62368900:62368900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983C>A
AA Mutation	p.Ser328Ter(p.S328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript