Colon Cancer: Gene >> NFE2L3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26184720:26184720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779702861
CDS Mutation	c.1022C>A
AA Mutation	p.Pro341Gln(p.P341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26185473:26185473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374797223
CDS Mutation	c.1775C>T
AA Mutation	p.Ala592Val(p.A592V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26185308:26185308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566561270
CDS Mutation	c.1610G>A
AA Mutation	p.Arg537His(p.R537H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26184917:26184917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219G>A
AA Mutation	p.Asp407Asn(p.D407N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26183740:26183740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790G>C
AA Mutation	p.Asp264His(p.D264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26185167:26185167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767647938
CDS Mutation	c.1469C>T
AA Mutation	p.Thr490Ile(p.T490I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26184952:26184952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254T>G
AA Mutation	p.Asp418Glu(p.D418E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26185634:26185634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551577266
CDS Mutation	c.1936T>G
AA Mutation	p.Phe646Val(p.F646V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26177953:26177953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581T>C
AA Mutation	p.Val194Ala(p.V194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000056233
Start	26185699:26185699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000056233
Start	26185655:26185656(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1959dupA
AA Mutation	p.Gly654ArgfsTer2(p.G654Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000056233
Start	26185626:26185628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776567501
CDS Mutation	c.1930_1932delGAT
AA Mutation	p.Asp644del(p.D644del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NFE2L3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000056233
Start	26185002:26185002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304C>G
AA Mutation	p.Ser435Cys(p.S435C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000056233
Start	26178009:26178009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>T
AA Mutation	p.Glu213Ter(p.E213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript