Colon Cancer: Gene >> TRIM69

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767561:44767561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292C>T
AA Mutation	p.Ser431Phe(p.S431F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44754934:44754934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41G>A
AA Mutation	p.Gly14Asp(p.G14D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767309:44767309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.His347Arg(p.H347R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767410:44767410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>A
AA Mutation	p.Glu381Lys(p.E381K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44759770:44759770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>A
AA Mutation	p.Leu287Met(p.L287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329464
Start	44767316:44767316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367675407
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329464
Start	44755115:44755115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329464
Start	44755055:44755055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000329464
Start	44754958:44754958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65C>A
AA Mutation	p.Ser22Ter(p.S22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM69

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44755315:44755315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749171075
CDS Mutation	c.422G>A
AA Mutation	p.Arg141Gln(p.R141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767341:44767341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372919928
CDS Mutation	c.1072C>T
AA Mutation	p.Pro358Ser(p.P358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767325:44767325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056G>T
AA Mutation	p.Lys352Asn(p.K352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44755037:44755037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768458983
CDS Mutation	c.144C>A
AA Mutation	p.Phe48Leu(p.F48L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329464
Start	44767470:44767470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201166045
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Trp(p.R401W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329464
Start	44754926:44754926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748470236
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000329464
Start	44767458:44767458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189G>T
AA Mutation	p.Glu397Ter(p.E397*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript