Colon Cancer: Gene >> NKD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268459
Start	50621652:50621652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310A>G
AA Mutation	p.Lys104Glu(p.K104E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268459
Start	50625569:50625569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>A
AA Mutation	p.Val151Ile(p.V151I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268459
Start	50633488:50633488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374394871
CDS Mutation	c.1120G>A
AA Mutation	p.Ala374Thr(p.A374T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268459
Start	50633304:50633304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000268459
Start	50633248:50633248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Ter(p.R294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268459
Start	50633223:50633224(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772439983
CDS Mutation	c.862dupC
AA Mutation	p.Arg288ProfsTer12(p.R288Pfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NKD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268459
Start	50630223:50630223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500T>G
AA Mutation	p.Val167Gly(p.V167G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268459
Start	50632329:50632329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777762024
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript