Colon Cancer: Gene >> KEAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10489670:10489670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509G>T
AA Mutation	p.Met503Ile(p.M503I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10499795:10499795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239C>T
AA Mutation	p.Thr80Ile(p.T80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10499541:10499541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752325770
CDS Mutation	c.493G>A
AA Mutation	p.Asp165Asn(p.D165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10500011:10500011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746950247
CDS Mutation	c.23G>A
AA Mutation	p.Ser8Asn(p.S8N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10499661:10499661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373A>G
AA Mutation	p.Ile125Val(p.I125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000171111
Start	10492235:10492235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>A
AA Mutation	p.Leu223Met(p.L223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000171111
Start	10500010:10500010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758239745
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000171111
Start	10492167:10492167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000171111
Start	10489226:10489226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KEAP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000171111
Start	10489787:10489787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763857137
CDS Mutation	c.1392C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000171111
Start	10499536:10499536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767150108
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript