Colon Cancer: Gene >> CNOT11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101257880:101257880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201833579
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Cys(p.R202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101257920:101257920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644C>A
AA Mutation	p.Ser215Tyr(p.S215Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101257931:101257931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750783059
CDS Mutation	c.655A>G
AA Mutation	p.Ser219Gly(p.S219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101269228:101269228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101257875:101257875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778787740
CDS Mutation	c.599C>T
AA Mutation	p.Thr200Met(p.T200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101262670:101262670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775090253
CDS Mutation	c.811G>A
AA Mutation	p.Gly271Arg(p.G271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101253040:101253040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76G>T
AA Mutation	p.Ala26Ser(p.A26S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101264995:101264995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CNOT11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289382
Start	101266683:101266683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042G>A
AA Mutation	p.Gly348Ser(p.G348S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript