Colon Cancer: Gene >> NFE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54292444:54292444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052C>T
AA Mutation	p.Ala351Val(p.A351V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54292822:54292822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768645314
CDS Mutation	c.674G>A
AA Mutation	p.Arg225Gln(p.R225Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54292465:54292465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031G>A
AA Mutation	p.Ser344Asn(p.S344N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54292702:54292702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794C>T
AA Mutation	p.Ala265Val(p.A265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54293179:54293179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317T>G
AA Mutation	p.Val106Gly(p.V106G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54293063:54293063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>A
AA Mutation	p.Asp145Asn(p.D145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312156
Start	54293145:54293145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312156
Start	54292669:54292669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.827delA
AA Mutation	p.Asn276ThrfsTer26(p.N276Tfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312156
Start	54292835:54292835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.661delG
AA Mutation	p.Glu221ArgfsTer13(p.E221Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000312156
Start	54293069:54293069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>T
AA Mutation	p.Glu143Ter(p.E143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312156
Start	54292745:54292746(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.750dupT
AA Mutation	p.Asn251Ter(p.N251*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NFE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54293036:54293036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460G>A
AA Mutation	p.Asp154Asn(p.D154N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312156
Start	54292850:54292850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646C>A
AA Mutation	p.Pro216Thr(p.P216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312156
Start	54293331:54293331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.165A>T
Mutation Classification	Silent
Feature Type	Transcript