Colon Cancer: Gene >> CNOT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54148263:54148263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010C>T
AA Mutation	p.Thr337Ile(p.T337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54149648:54149648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495C>T
AA Mutation	p.Pro499Ser(p.P499S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54152961:54152961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999T>C
AA Mutation	p.Ser667Pro(p.S667P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54152265:54152265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Trp(p.R549W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54148460:54148460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207A>C
AA Mutation	p.Ser403Arg(p.S403R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54152619:54152619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897C>T
AA Mutation	p.Arg633Cys(p.R633C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221232
Start	54152966:54152966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221232
Start	54148483:54148483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749896898
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221232
Start	54146013:54146013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221232
Start	54148705:54148705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1373delC
AA Mutation	p.Pro458LeufsTer45(p.P458Lfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CNOT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221232
Start	54148442:54148442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765712541
CDS Mutation	c.1189G>A
AA Mutation	p.Gly397Arg(p.G397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221232
Start	54148195:54148195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942T>G
Mutation Classification	Silent
Feature Type	Transcript