Colon Cancer: Gene >> FOXK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4754487:4754487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762929883
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Cys(p.R259C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4759554:4759554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1655C>T
AA Mutation	p.Ala552Val(p.A552V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4759406:4759406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Val503Ile(p.V503I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4754572:4754572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200047032
CDS Mutation	c.860C>T
AA Mutation	p.Ala287Val(p.A287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4762219:4762219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957G>T
AA Mutation	p.Ala653Ser(p.A653S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4757069:4757069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>T
AA Mutation	p.Gly376Trp(p.G376W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4755253:4755253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370103596
CDS Mutation	c.920C>T
AA Mutation	p.Pro307Leu(p.P307L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4759536:4759536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778526385
CDS Mutation	c.1637C>T
AA Mutation	p.Ala546Val(p.A546V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000328914
Start	4762186:4762186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1924C>A
AA Mutation	p.Leu642Ile(p.L642I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4761225:4761225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762122739
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Trp(p.R620W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4757040:4757040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097T>C
AA Mutation	p.Val366Ala(p.V366A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4761088:4761088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1721C>T
AA Mutation	p.Ala574Val(p.A574V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4759463:4759463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1564G>A
AA Mutation	p.Val522Ile(p.V522I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4740842:4740842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565A>G
AA Mutation	p.Thr189Ala(p.T189A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4757180:4757180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237T>C
AA Mutation	p.Ser413Pro(p.S413P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4761226:4761226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373966273
CDS Mutation	c.1859G>A
AA Mutation	p.Arg620Gln(p.R620Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4761229:4761229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862C>T
AA Mutation	p.Ala621Val(p.A621V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4757132:4757132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Trp(p.R397W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4762299:4762299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111856572
CDS Mutation	c.2037G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4759210:4759210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770027556
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4759576:4759576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1677C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4755263:4755263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200771103
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328914
Start	4740930:4740931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.654_655delGT
AA Mutation	p.Tyr219ProfsTer84(p.Y219Pfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000328914
Start	4682771:4682771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463G>T
AA Mutation	p.Glu155Ter(p.E155*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000328914
Start	4761290:4761290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FOXK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328914
Start	4757003:4757003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Trp(p.R354W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4755305:4755305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4762236:4762236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570756478
CDS Mutation	c.1974G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328914
Start	4740886:4740886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763587560
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328914
Start	4759088:4759089(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1286dupC
AA Mutation	p.Arg430SerfsTer23(p.R430Sfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript