Colon Cancer: Gene >> KIF2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44761979:44761979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747G>A
AA Mutation	p.Asp583Asn(p.D583N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44756230:44756230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970G>A
AA Mutation	p.Val324Ile(p.V324I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44758085:44758085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169A>T
AA Mutation	p.Tyr390Phe(p.Y390F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44767103:44767103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102T>A
AA Mutation	p.Ile701Asn(p.I701N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44758070:44758070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154A>C
AA Mutation	p.Lys385Thr(p.K385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44756178:44756178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918C>A
AA Mutation	p.Asn306Lys(p.N306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44750495:44750495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44759239:44759239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258C>T
AA Mutation	p.Arg420Cys(p.R420C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372224
Start	44754844:44754844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758C>A
AA Mutation	p.Pro253His(p.P253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44754810:44754810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724A>C
AA Mutation	p.Thr242Pro(p.T242P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372224
Start	44760451:44760451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144656043
CDS Mutation	c.1539C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372224
Start	44753138:44753139(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.446_447insA
AA Mutation	p.Thr150HisfsTer2(p.T150Hfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44750544:44750544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200680875
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44762435:44762435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199917085
CDS Mutation	c.1841C>T
AA Mutation	p.Ala614Val(p.A614V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44747396:44747396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>T
AA Mutation	p.Asp60Tyr(p.D60Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372224
Start	44757606:44757606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028C>A
AA Mutation	p.Thr343Asn(p.T343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372224
Start	44756220:44756220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146490098
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript