Colon Cancer: Gene >> NEK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211669211:211669211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887C>T
AA Mutation	p.Ser296Leu(p.S296L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366999
Start	211673484:211673484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554C>T
AA Mutation	p.Pro185Leu(p.P185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211669190:211669190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908T>C
AA Mutation	p.Leu303Ser(p.L303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211674380:211674380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767290689
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211673605:211673605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366999
Start	211669267:211669267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143249148
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211673511:211673511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527T>G
AA Mutation	p.Phe176Cys(p.F176C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366999
Start	211663496:211663496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423Gln(p.R423Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript