Colon Cancer: Gene >> CNOT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361272
Start	17234777:17234777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361272
Start	17232473:17232473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683G>A
AA Mutation	p.Gly228Glu(p.G228E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361272
Start	17234821:17234821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361272
Start	17237310:17237310(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.375delA
AA Mutation	p.Lys125AsnfsTer17(p.K125Nfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000361272
Start	17237273:17237273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>T
AA Mutation	p.Glu138Ter(p.E138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000361272
Start	17237255:17237255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Gly144Ter(p.G144*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000361272
Start	17237226:17237226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459G>A
AA Mutation	p.Trp153Ter(p.W153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361272
Start	17234766:17234767(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.567dupT
AA Mutation	p.Pro190SerfsTer5(p.P190Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CNOT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361272
Start	17245058:17245058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375278542
CDS Mutation	c.95G>A
AA Mutation	p.Arg32Gln(p.R32Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript