Colon Cancer: Gene >> TRIM28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58545477:58545477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>T
AA Mutation	p.Glu131Asp(p.E131D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58549995:58549995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2153G>A
AA Mutation	p.Arg718His(p.R718H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58549496:58549496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1828G>T
AA Mutation	p.Gly610Cys(p.G610C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58549953:58549953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2111G>A
AA Mutation	p.Cys704Tyr(p.C704Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58548901:58548901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400G>A
AA Mutation	p.Gly467Asp(p.G467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253024
Start	58549984:58549984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756462692
CDS Mutation	c.2142C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253024
Start	58549996:58549996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2154C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000253024
Start	58549037:58549037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459C>T
AA Mutation	p.Arg487Ter(p.R487*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253024
Start	58549985:58549985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780327650
CDS Mutation	c.2143G>A
AA Mutation	p.Glu715Lys(p.E715K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253024
Start	58549189:58549189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142762100
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript