Colon Cancer: Gene >> NLK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407008
Start	28168596:28168596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>A
AA Mutation	p.Cys329Tyr(p.C329Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407008
Start	28122616:28122616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>T
AA Mutation	p.Pro158Ser(p.P158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407008
Start	28168457:28168457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847T>G
AA Mutation	p.Phe283Val(p.F283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407008
Start	28042927:28042927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143100809
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407008
Start	28168651:28168651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407008
Start	28042957:28042957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407008
Start	28122714:28122714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.576delT
AA Mutation	p.Phe192LeufsTer30(p.F192Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NLK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407008
Start	28161245:28161245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730T>A
AA Mutation	p.Phe244Ile(p.F244I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407008
Start	28122714:28122714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570T>C
Mutation Classification	Silent
Feature Type	Transcript