Colon Cancer: Gene >> NUAK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367157
Start	205308655:205308655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201895375
CDS Mutation	c.430C>T
AA Mutation	p.Arg144Trp(p.R144W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367157
Start	205311782:205311782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>G
AA Mutation	p.Gln92Arg(p.Q92R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367157
Start	205308636:205308636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558886995
CDS Mutation	c.449G>A
AA Mutation	p.Arg150His(p.R150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367157
Start	205303947:205303947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390G>A
AA Mutation	p.Glu464Lys(p.E464K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367157
Start	205308618:205308618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467T>C
AA Mutation	p.Phe156Ser(p.F156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367157
Start	205303825:205303825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367157
Start	205304089:205304089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367157
Start	205306206:205306206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367157
Start	205308635:205308635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374444303
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000367157
Start	205303671:205303671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1666C>T
AA Mutation	p.Gln556Ter(p.Q556*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NUAK2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367157
Start	205308707:205308710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.375_378delCGTG
AA Mutation	p.Val126SerfsTer132(p.V126Sfs*132)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript