Colon Cancer: Gene >> KIF23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69423190:69423190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595A>G
AA Mutation	p.Ile199Val(p.I199V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69444848:69444848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191196584
CDS Mutation	c.2438G>A
AA Mutation	p.Arg813His(p.R813H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69444826:69444826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416C>T
AA Mutation	p.Arg806Cys(p.R806C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69440850:69440850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150G>A
AA Mutation	p.Cys717Tyr(p.C717Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69426168:69426168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833A>C
AA Mutation	p.Glu278Ala(p.E278A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260363
Start	69440313:69440313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1893T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260363
Start	69436673:69436673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260363
Start	69435729:69435730(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1238_1239dupTG
AA Mutation	p.Asn414Ter(p.N414*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000260363
Start	69445043:69445043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2631+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KIF23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69444826:69444826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416C>T
AA Mutation	p.Arg806Cys(p.R806C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260363
Start	69426145:69426145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810G>T
Mutation Classification	Silent
Feature Type	Transcript