Colon Cancer: Gene >> NOB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268802
Start	69749289:69749289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>T
AA Mutation	p.Glu150Val(p.E150V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268802
Start	69742430:69742430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145274258
CDS Mutation	c.1141C>T
AA Mutation	p.Arg381Cys(p.R381C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268802
Start	69742491:69742491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375136678
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000268802
Start	69742579:69742580(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.991_992insTCA
AA Mutation	p.Gly331delinsValArg(p.G331delinsVR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOB1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268802
Start	69744945:69744945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201462080
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000268802
Start	69742569:69742570(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1001dupA
AA Mutation	p.Tyr334Ter(p.Y334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000268802
Start	69748231:69748231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript