Colon Cancer: Gene >> NEK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320246
Start	124327382:124327382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>C
AA Mutation	p.Lys187Gln(p.K187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320246
Start	124347802:124347802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779084313
CDS Mutation	c.811G>A
AA Mutation	p.Gly271Arg(p.G271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320246
Start	124350862:124350862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857T>C
AA Mutation	p.Ile286Thr(p.I286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320246
Start	124312546:124312546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183673274
CDS Mutation	c.128C>T
AA Mutation	p.Ala43Val(p.A43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320246
Start	124327378:124327378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320246
Start	124327405:124327405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320246
Start	124321503:124321503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765205974
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320246
Start	124321542:124321542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779446532
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320246
Start	124312541:124312541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766708819
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEK6

No Mutation Annotation!