Colon Cancer: Gene >> KDM4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5041184:5041184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365A>G
AA Mutation	p.Tyr122Cys(p.Y122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131301:5131301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541C>A
AA Mutation	p.Pro514His(p.P514H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5047533:5047533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490G>A
AA Mutation	p.Glu164Lys(p.E164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131135:5131135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375T>G
AA Mutation	p.Phe459Val(p.F459V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5132004:5132004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903G>A
AA Mutation	p.Glu635Lys(p.E635K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5039846:5039846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152C>T
AA Mutation	p.Pro51Leu(p.P51L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131433:5131433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673G>A
AA Mutation	p.Gly558Asp(p.G558D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131268:5131268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771331474
CDS Mutation	c.1508C>T
AA Mutation	p.Pro503Leu(p.P503L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131933:5131933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Gln(p.R611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5133969:5133969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1993G>A
AA Mutation	p.Ala665Thr(p.A665T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5144295:5144295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2784G>T
AA Mutation	p.Lys928Asn(p.K928N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131472:5131472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750077858
CDS Mutation	c.1712C>T
AA Mutation	p.Thr571Met(p.T571M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131234:5131234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1474C>A
AA Mutation	p.Pro492Thr(p.P492T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5110723:5110723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142922912
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5144095:5144095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764846218
CDS Mutation	c.2679C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5144071:5144071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768208492
CDS Mutation	c.2655C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5110762:5110762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139508576
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5039844:5039844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5131952:5131952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5144331:5144331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747587630
CDS Mutation	c.2820C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5077395:5077395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202178470
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5143972:5143972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2556C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5144077:5144077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776115281
CDS Mutation	c.2661C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5131350:5131350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200099448
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5131892:5131892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544835411
CDS Mutation	c.1791G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5135473:5135473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768283280
CDS Mutation	c.2220G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5110762:5110762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5135461:5135461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2208C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159111
Start	5131288:5131288(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1532delC
AA Mutation	p.Pro511LeufsTer8(p.P511Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KDM4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5151345:5151345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200961372
CDS Mutation	c.3125C>T
AA Mutation	p.Thr1042Met(p.T1042M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131082:5131082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Gly441Glu(p.G441E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5110702:5110702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999G>T
AA Mutation	p.Trp333Cys(p.W333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5047532:5047532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754414783
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5047565:5047565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript