Colon Cancer: Gene >> NEK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28734837:28734837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.His107Tyr(p.H107Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28737966:28737966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037G>A
AA Mutation	p.Gly346Asp(p.G346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28734921:28734921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>A
AA Mutation	p.Leu135Met(p.L135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28737876:28737876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947C>G
AA Mutation	p.Ala316Gly(p.A316G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28741523:28741523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002G>A
AA Mutation	p.Val668Met(p.V668M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28734963:28734963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>A
AA Mutation	p.Gly149Ser(p.G149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28740853:28740853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600C>A
AA Mutation	p.Leu534Met(p.L534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28741112:28741112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767G>C
AA Mutation	p.Gln589His(p.Q589H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268766
Start	28737877:28737877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268766
Start	28741978:28741978(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2076delC
AA Mutation	p.Ter693GlufsTer11(p.*693Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268766
Start	28741977:28741978(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs755820155
CDS Mutation	c.2076dupC
AA Mutation	p.Ter693LeufsTer86(p.*693Lfs*86)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NEK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28737364:28737364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268766
Start	28734068:28734068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Trp(p.R45W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript