Colon Cancer: Gene >> NFKB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102396299:102396299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>A
AA Mutation	p.Ser23Tyr(p.S23Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102398047:102398047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728G>A
AA Mutation	p.Gly243Glu(p.G243E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102400796:102400796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940T>C
AA Mutation	p.Leu647Pro(p.L647P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102401801:102401801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367889547
CDS Mutation	c.2350G>A
AA Mutation	p.Gly784Arg(p.G784R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102401766:102401766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2315A>G
AA Mutation	p.Asp772Gly(p.D772G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369966
Start	102402274:102402274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369966
Start	102400472:102400472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1779G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369966
Start	102398406:102398406(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.879delC
AA Mutation	p.Tyr294IlefsTer4(p.Y294Ifs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369966
Start	102401179:102401179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2072-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NFKB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102400393:102400393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199841036
CDS Mutation	c.1700C>T
AA Mutation	p.Ala567Val(p.A567V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102402057:102402057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2476G>A
AA Mutation	p.Gly826Arg(p.G826R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369966
Start	102396735:102396735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155G>A
AA Mutation	p.Arg52Gln(p.R52Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript