Colon Cancer: Gene >> NFE2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48059018:48059018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696C>T
AA Mutation	p.Pro566Ser(p.P566S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48059190:48059190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868T>C
AA Mutation	p.Ile623Thr(p.I623T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48059271:48059271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949C>G
AA Mutation	p.Ala650Gly(p.A650G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48058313:48058313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991T>C
AA Mutation	p.Ser331Pro(p.S331P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48057484:48057484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.954G>A
AA Mutation	p.Met318Ile(p.M318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48058550:48058550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228T>G
AA Mutation	p.Ser410Ala(p.S410A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48059559:48059559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2237G>A
AA Mutation	p.Gly746Asp(p.G746D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48058572:48058572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>C
AA Mutation	p.Phe417Ser(p.F417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48058911:48058911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589C>G
AA Mutation	p.Ser530Cys(p.S530C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48058629:48058629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307A>G
AA Mutation	p.Asp436Gly(p.D436G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362042
Start	48059551:48059551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766791282
CDS Mutation	c.2229C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362042
Start	48058426:48058426(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1109delG
AA Mutation	p.Gly370AlafsTer44(p.G370Afs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362042
Start	48051597:48051597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.485delC
AA Mutation	p.Pro162GlnfsTer6(p.P162Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NFE2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362042
Start	48051248:48051248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130C>A
AA Mutation	p.Leu44Met(p.L44M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript