Colon Cancer: Gene >> TRIM29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120125759:120125759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768839001
CDS Mutation	c.1265G>A
AA Mutation	p.Arg422His(p.R422H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120120601:120120601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1500G>T
AA Mutation	p.Lys500Asn(p.K500N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137772:120137772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260A>C
AA Mutation	p.Asp87Ala(p.D87A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120125840:120125840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184C>T
AA Mutation	p.Thr395Ile(p.T395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120128407:120128407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557844201
CDS Mutation	c.893G>A
AA Mutation	p.Arg298His(p.R298H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120115350:120115350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692G>T
AA Mutation	p.Lys564Asn(p.K564N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120115396:120115396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375996169
CDS Mutation	c.1646G>A
AA Mutation	p.Arg549Gln(p.R549Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120127478:120127478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535733632
CDS Mutation	c.992C>T
AA Mutation	p.Ala331Val(p.A331V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137665:120137665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>A
AA Mutation	p.Glu123Lys(p.E123K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137325:120137325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707G>A
AA Mutation	p.Cys236Tyr(p.C236Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120137927:120137927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120112426:120112426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533478417
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120127552:120127552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341846
Start	120125817:120125817(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1207delG
AA Mutation	p.Glu403ArgfsTer7(p.E403Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120115368:120115368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1674G>T
AA Mutation	p.Gln558His(p.Q558H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120123024:120123024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137882673
CDS Mutation	c.1365G>A
Mutation Classification	Silent
Feature Type	Transcript