Colon Cancer: Gene >> TNFRSF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12104465:12104465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764000451
CDS Mutation	c.355G>A
AA Mutation	p.Val119Ile(p.V119I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12104505:12104505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370304432
CDS Mutation	c.395C>T
AA Mutation	p.Pro132Leu(p.P132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12126198:12126198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271A>G
AA Mutation	p.Tyr424Cys(p.Y424C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12104436:12104436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326G>T
AA Mutation	p.Arg109Leu(p.R109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12138245:12138245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756257010
CDS Mutation	c.1352C>T
AA Mutation	p.Ala451Val(p.A451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263932
Start	12097160:12097160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211C>T
AA Mutation	p.Pro71Ser(p.P71S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12097123:12097123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12110131:12110131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12126202:12126202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12138417:12138417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12110155:12110155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000263932
Start	12138334:12138334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>T
AA Mutation	p.Glu481Ter(p.E481*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263932
Start	12112015:12112015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12097111:12097111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780251741
CDS Mutation	c.162G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12123781:12123781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202227728
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263932
Start	12115626:12115626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript