Colon Cancer: Gene >> KIF15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44775291:44775291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201137952
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Cys(p.R34C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44802832:44802832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528G>T
AA Mutation	p.Val510Phe(p.V510F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44838333:44838333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3230A>G
AA Mutation	p.Glu1077Gly(p.E1077G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44801499:44801499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272C>A
AA Mutation	p.Phe424Leu(p.F424L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44812273:44812273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261C>T
AA Mutation	p.Ser754Phe(p.S754F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44774403:44774403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369068128
CDS Mutation	c.28C>T
AA Mutation	p.Arg10Cys(p.R10C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44828268:44828268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371462063
CDS Mutation	c.2911A>G
AA Mutation	p.Ser971Gly(p.S971G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44797570:44797570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44827487:44827487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2815C>T
AA Mutation	p.Arg939Cys(p.R939C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44775362:44775362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758234349
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44786448:44786448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148032198
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44851853:44851853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326047
Start	44794392:44794392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.819delA
AA Mutation	p.Asp274IlefsTer7(p.D274Ifs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326047
Start	44794245:44794245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.668delG
AA Mutation	p.Arg223LeufsTer7(p.R223Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326047
Start	44801807:44801807(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1346delA
AA Mutation	p.Lys449ArgfsTer10(p.K449Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000326047
Start	44805035:44805035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696G>T
AA Mutation	p.Gly566Ter(p.G566*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326047
Start	44848041:44848042(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3752_3753insTTTCAAATTC
AA Mutation	p.Lys1251AsnfsTer11(p.K1251Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44841170:44841170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3517T>G
AA Mutation	p.Leu1173Val(p.L1173V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326047
Start	44838343:44838343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3240A>T
AA Mutation	p.Lys1080Asn(p.K1080N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44851853:44851853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44800361:44800361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326047
Start	44805950:44805950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935T>C
Mutation Classification	Silent
Feature Type	Transcript