Colon Cancer: Gene >> TRIM58

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247864886:247864886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777618771
CDS Mutation	c.698C>T
AA Mutation	p.Ala233Val(p.A233V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247857381:247857381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>T
AA Mutation	p.Glu45Asp(p.E45D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247868018:247868018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>A
AA Mutation	p.Ala276Thr(p.A276T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247876182:247876182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>T
AA Mutation	p.Trp385Leu(p.W385L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247876146:247876146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118C>T
AA Mutation	p.Thr373Ile(p.T373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247857412:247857412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247857370:247857370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Glu42Lys(p.E42K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247876440:247876440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412C>A
AA Mutation	p.Ser471Tyr(p.S471Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247876114:247876114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247875919:247875919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745534672
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247857288:247857288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247857402:247857402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM58

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247860697:247860697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>T
AA Mutation	p.Lys167Asn(p.K167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366481
Start	247875998:247875998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970A>G
AA Mutation	p.Asn324Asp(p.N324D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247867850:247867850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247864761:247864761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366481
Start	247864785:247864785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript