Colon Cancer: Gene >> KIF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39545614:39545614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780284536
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419His(p.R419H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287152
Start	39420001:39420001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757T>G
AA Mutation	p.Phe586Cys(p.F586C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39431063:39431063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744C>A
AA Mutation	p.Leu582Met(p.L582M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39360520:39360520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1957A>T
AA Mutation	p.Met653Leu(p.M653L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39540029:39540029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619G>T
AA Mutation	p.Arg540Ile(p.R540I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39545641:39545641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229G>A
AA Mutation	p.Ser410Asn(p.S410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39431130:39431130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1677G>T
AA Mutation	p.Gln559His(p.Q559H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39540158:39540158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765089235
CDS Mutation	c.1490G>A
AA Mutation	p.Gly497Asp(p.G497D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39720771:39720771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107T>C
AA Mutation	p.Leu36Ser(p.L36S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39545664:39545664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206T>G
AA Mutation	p.Phe402Leu(p.F402L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39578063:39578063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174C>T
AA Mutation	p.Leu392Phe(p.L392F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39714758:39714758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.185G>T
AA Mutation	p.Arg62Ile(p.R62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39586398:39586398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853A>G
AA Mutation	p.Ile285Val(p.I285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39596108:39596108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39343779:39343779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767373723
CDS Mutation	c.2358C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39639706:39639706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371477997
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39431082:39431082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39586399:39586399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287152
Start	39613217:39613217(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.611delT
AA Mutation	p.Leu204Ter(p.L204*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000287152
Start	39540081:39540081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145150015
CDS Mutation	c.1567C>T
AA Mutation	p.Arg523Ter(p.R523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000287152
Start	39584985:39584985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KIF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39385646:39385646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139112928
CDS Mutation	c.1837C>T
AA Mutation	p.Arg613Trp(p.R613W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39357335:39357335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372001923
CDS Mutation	c.2122C>T
AA Mutation	p.Pro708Ser(p.P708S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39540065:39540065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583C>T
AA Mutation	p.Pro528Leu(p.P528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287152
Start	39343795:39343795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180943940
CDS Mutation	c.2342C>T
AA Mutation	p.Ser781Leu(p.S781L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39360509:39360509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1968C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287152
Start	39360485:39360485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript