Colon Cancer: Gene >> KIF22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29802890:29802890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779821702
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Trp(p.R468W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29803557:29803557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558G>A
AA Mutation	p.Val520Ile(p.V520I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29798721:29798721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523T>C
AA Mutation	p.Ser175Pro(p.S175P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29802885:29802885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145879411
CDS Mutation	c.1397G>A
AA Mutation	p.Arg466Gln(p.R466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29804932:29804932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796G>A
AA Mutation	p.Gly599Asp(p.G599D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000160827
Start	29799488:29799488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000160827
Start	29802799:29802799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000160827
Start	29803465:29803465(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1470delA
AA Mutation	p.Glu491AsnfsTer36(p.E491Nfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000160827
Start	29799963:29799964(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1196_1203dupCAAAGAGA
AA Mutation	p.Ala402GlnfsTer34(p.A402Qfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000160827
Start	29798484:29798484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764389481
CDS Mutation	c.377A>G
AA Mutation	p.Tyr126Cys(p.Y126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000160827
Start	29804905:29804905(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1774delA
AA Mutation	p.Ile592TyrfsTer5(p.I592Yfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript