Colon Cancer: Gene >> KIF5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32018102:32018102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2494A>G
AA Mutation	p.Ile832Val(p.I832V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32021240:32021240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2080G>A
AA Mutation	p.Ala694Thr(p.A694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302418
Start	32035667:32035667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817A>G
AA Mutation	p.Thr273Ala(p.T273A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32028524:32028524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629G>A
AA Mutation	p.Met543Ile(p.M543I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32017230:32017230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773585260
CDS Mutation	c.2674C>T
AA Mutation	p.Arg892Cys(p.R892C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32035961:32035961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>A
AA Mutation	p.Asp249Asn(p.D249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32033934:32033934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377656602
CDS Mutation	c.1216G>A
AA Mutation	p.Ala406Thr(p.A406T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32031229:32031229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1425T>A
AA Mutation	p.Asn475Lys(p.N475K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32017236:32017236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760268366
CDS Mutation	c.2668C>T
AA Mutation	p.Arg890Cys(p.R890C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32015535:32015535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2886A>T
AA Mutation	p.Gln962His(p.Q962H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32034832:32034832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969A>C
AA Mutation	p.Lys323Asn(p.K323N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302418
Start	32022898:32022898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1864delA
AA Mutation	p.Met622TrpfsTer8(p.M622Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302418
Start	32037283:32037284(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.681_682delTT
AA Mutation	p.Tyr228SerfsTer3(p.Y228Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000302418
Start	32017358:32017358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2546T>A
AA Mutation	p.Leu849Ter(p.L849*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000302418
Start	32033880:32033880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270G>T
AA Mutation	p.Glu424Ter(p.E424*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000302418
Start	32018381:32018381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2374G>T
AA Mutation	p.Glu792Ter(p.E792*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KIF5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32022858:32022858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369345488
CDS Mutation	c.1904G>A
AA Mutation	p.Arg635His(p.R635H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32017224:32017224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141491660
CDS Mutation	c.2680C>T
AA Mutation	p.Arg894Cys(p.R894C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32021098:32021098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2128G>A
AA Mutation	p.Glu710Lys(p.E710K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32022859:32022859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1903C>T
AA Mutation	p.Arg635Cys(p.R635C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32035651:32035651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32037574:32037574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532G>A
AA Mutation	p.Glu178Lys(p.E178K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302418
Start	32018545:32018545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201506716
CDS Mutation	c.2324G>A
AA Mutation	p.Arg775Gln(p.R775Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000302418
Start	32018381:32018381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2374G>T
AA Mutation	p.Glu792Ter(p.E792*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000302418
Start	32034756:32034756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>T
AA Mutation	p.Glu349Ter(p.E349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript