Colon Cancer: Gene >> NFE2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177233273:177233273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379T>A
AA Mutation	p.Phe127Ile(p.F127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177230897:177230897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765321668
CDS Mutation	c.1706G>A
AA Mutation	p.Arg569His(p.R569H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177230879:177230879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724C>T
AA Mutation	p.Pro575Leu(p.P575L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177232579:177232579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407C>A
AA Mutation	p.Ser136Tyr(p.S136Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177230916:177230916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763240080
CDS Mutation	c.1687G>A
AA Mutation	p.Glu563Lys(p.E563K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177230957:177230957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765842312
CDS Mutation	c.1646G>T
AA Mutation	p.Ser549Ile(p.S549I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177230990:177230990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613A>C
AA Mutation	p.Lys538Thr(p.K538T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NFE2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177231563:177231563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>T
AA Mutation	p.Ser347Leu(p.S347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177231071:177231071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532C>T
AA Mutation	p.Ala511Val(p.A511V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397062
Start	177233281:177233281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749353894
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397062
Start	177234104:177234104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775813661
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000397062
Start	177231465:177231465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>T
AA Mutation	p.Glu380Ter(p.E380*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript