Colon Cancer: Gene >> MSRB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65326885:65326885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568898551
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65328546:65328546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227C>T
AA Mutation	p.Thr76Ile(p.T76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65463266:65463266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142488075
CDS Mutation	c.523G>A
AA Mutation	p.Ala175Thr(p.A175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65453774:65453774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>A
AA Mutation	p.Phe120Leu(p.F120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65463209:65463209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466A>G
AA Mutation	p.Arg156Gly(p.R156G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65463225:65463225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603630
CDS Mutation	c.482C>T
AA Mutation	p.Ser161Leu(p.S161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355192
Start	65278834:65278834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355192
Start	65278858:65278858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355192
Start	65463312:65463313(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.569_570insA
AA Mutation	p.Glu191GlyfsTer5(p.E191Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355192
Start	65463313:65463314(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.571_572insCTTTG
AA Mutation	p.Glu191AlafsTer29(p.E191Afs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MSRB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65328530:65328530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211T>A
AA Mutation	p.Phe71Ile(p.F71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355192
Start	65328548:65328548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>G
AA Mutation	p.His77Asp(p.H77D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355192
Start	65453759:65453759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345T>G
Mutation Classification	Silent
Feature Type	Transcript