Colon Cancer: Gene >> TRIM27

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377199
Start	28908975:28908975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884C>T
AA Mutation	p.Thr295Ile(p.T295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377199
Start	28921953:28921953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455G>C
AA Mutation	p.Arg152Thr(p.R152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377199
Start	28923606:28923606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770219998
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377199
Start	28904559:28904559(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1053delC
AA Mutation	p.Glu352ArgfsTer24(p.E352Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377199
Start	28908835:28908835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.892delA
AA Mutation	p.Met298CysfsTer11(p.M298Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377199
Start	28921927:28921927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763531927
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Trp(p.R161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377199
Start	28923499:28923499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Gly45Asp(p.G45D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript