Colon Cancer: Gene >> NUCKS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367142
Start	205720609:205720609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754971187
CDS Mutation	c.274C>A
AA Mutation	p.Gln92Lys(p.Q92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367142
Start	205727784:205727784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762593780
CDS Mutation	c.89C>T
AA Mutation	p.Ser30Leu(p.S30L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367142
Start	205723937:205723937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>A
AA Mutation	p.Ser73Tyr(p.S73Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367142
Start	205723951:205723951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367142
Start	205727783:205727783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775426197
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NUCKS1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367142
Start	205719612:205719612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753207169
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367142
Start	205723975:205723975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000367142
Start	205729600:205729600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>A
AA Mutation	p.Tyr13Ter(p.Y13*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript