Colon Cancer: Gene >> KIFC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33406218:33406218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1559C>G
AA Mutation	p.Ala520Gly(p.A520G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33404028:33404028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570330144
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Trp(p.R219W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33406259:33406259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373384743
CDS Mutation	c.1600C>T
AA Mutation	p.Arg534Trp(p.R534W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33406269:33406269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1610G>A
AA Mutation	p.Arg537His(p.R537H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33405474:33405474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379G>T
AA Mutation	p.Ser460Ile(p.S460I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33403994:33403994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>T
AA Mutation	p.Lys207Asn(p.K207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33406452:33406452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793C>T
AA Mutation	p.Thr598Met(p.T598M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000428849
Start	33404066:33404067(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.699dupA
AA Mutation	p.Gln234ThrfsTer52(p.Q234Tfs*52)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIFC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428849
Start	33405168:33405168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1073G>C
AA Mutation	p.Gly358Ala(p.G358A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000428849
Start	33398033:33398033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763606695
CDS Mutation	c.22delC
AA Mutation	p.Leu8TyrfsTer4(p.L8Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript