Colon Cancer: Gene >> KIF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92633728:92633728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808T>G
AA Mutation	p.Ile603Ser(p.I603S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92648302:92648302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2638T>G
AA Mutation	p.Phe880Val(p.F880V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260731
Start	92606715:92606715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>T
AA Mutation	p.Ala103Ser(p.A103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92650507:92650507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3029C>A
AA Mutation	p.Pro1010Gln(p.P1010Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92613107:92613107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Val256Ile(p.V256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92593380:92593380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260731
Start	92606690:92606690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260731
Start	92637397:92637397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2018delA
AA Mutation	p.Lys673ArgfsTer3(p.K673Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000260731
Start	92630248:92630248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>T
AA Mutation	p.Glu460Ter(p.E460*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260731
Start	92609477:92609478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.666_667insTCCATTAG
AA Mutation	p.Thr223SerfsTer8(p.T223Sfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92645554:92645554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2459A>C
AA Mutation	p.Glu820Ala(p.E820A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92609096:92609096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464C>T
AA Mutation	p.Ser155Leu(p.S155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92648239:92648239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575A>C
AA Mutation	p.Ser859Arg(p.S859R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260731
Start	92609062:92609062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430T>A
AA Mutation	p.Phe144Ile(p.F144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000260731
Start	92630248:92630248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>T
AA Mutation	p.Glu460Ter(p.E460*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript