Colon Cancer: Gene >> NIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394140
Start	100355201:100355201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373969032
CDS Mutation	c.764G>A
AA Mutation	p.Arg255His(p.R255H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394140
Start	100339198:100339198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119C>A
AA Mutation	p.Ser40Tyr(p.S40Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000394140
Start	100339207:100339207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394140
Start	100345630:100345630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>A
AA Mutation	p.Glu128Lys(p.E128K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000394140
Start	100345630:100345630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>T
AA Mutation	p.Glu128Ter(p.E128*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript