Colon Cancer: Gene >> TRIM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102656855:102656855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157C>T
AA Mutation	p.Ala386Val(p.A386V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102656915:102656915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1217C>T
AA Mutation	p.Ala406Val(p.A406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102654677:102654677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747235303
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Trp(p.R199W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102656840:102656840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751046151
CDS Mutation	c.1142C>T
AA Mutation	p.Thr381Met(p.T381M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102655110:102655110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Trp(p.R233W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102657232:102657232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772676859
CDS Mutation	c.1534G>A
AA Mutation	p.Val512Ile(p.V512I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302424
Start	102656799:102656799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41300235
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302424
Start	102656907:102656907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000302424
Start	102657206:102657206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1508C>G
AA Mutation	p.Ser503Ter(p.S503*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302424
Start	102655196:102655196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783C>A
AA Mutation	p.Phe261Leu(p.F261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript