Colon Cancer: Gene >> KDM6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7847606:7847606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318C>T
AA Mutation	p.Pro440Ser(p.P440S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7853340:7853340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4868G>A
AA Mutation	p.Arg1623His(p.R1623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7852548:7852548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4522G>A
AA Mutation	p.Val1508Ile(p.V1508I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7847852:7847852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768893856
CDS Mutation	c.1564C>T
AA Mutation	p.Arg522Cys(p.R522C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7849533:7849533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762371888
CDS Mutation	c.3245C>T
AA Mutation	p.Pro1082Leu(p.P1082L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7849238:7849238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2950C>T
AA Mutation	p.Arg984Trp(p.R984W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7845895:7845895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756544042
CDS Mutation	c.161C>A
AA Mutation	p.Pro54His(p.P54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7853086:7853086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4697G>A
AA Mutation	p.Arg1566His(p.R1566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7852169:7852169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4301C>T
AA Mutation	p.Thr1434Met(p.T1434M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7845667:7845667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531880923
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7847883:7847883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532His(p.R532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7853058:7853058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4669G>A
AA Mutation	p.Ala1557Thr(p.A1557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7846098:7846098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257T>C
AA Mutation	p.Leu86Pro(p.L86P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000448097
Start	7847547:7847547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>A
AA Mutation	p.Pro420His(p.P420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7851074:7851074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368880082
CDS Mutation	c.3727G>A
AA Mutation	p.Val1243Met(p.V1243M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7851221:7851221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3874C>G
AA Mutation	p.Leu1292Val(p.L1292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7849566:7849566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202119281
CDS Mutation	c.3278G>A
AA Mutation	p.Arg1093His(p.R1093H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448097
Start	7849363:7849363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3075C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448097
Start	7848826:7848826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147289925
CDS Mutation	c.2538C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448097
Start	7848442:7848442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766690832
CDS Mutation	c.2154C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7847819:7847819(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747555402
CDS Mutation	c.1537delC
AA Mutation	p.Arg513AlafsTer69(p.R513Afs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7849583:7849583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3300delC
AA Mutation	p.Lys1101ArgfsTer3(p.K1101Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7848808:7848808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2525delC
AA Mutation	p.Pro842HisfsTer52(p.P842Hfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7848510:7848510(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2226delC
AA Mutation	p.Thr743ProfsTer39(p.T743Pfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7845657:7845657(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.107delC
AA Mutation	p.Pro36LeufsTer162(p.P36Lfs*162)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000448097
Start	7853330:7853330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4858G>T
AA Mutation	p.Glu1620Ter(p.E1620*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7847912:7847913(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1628dupC
AA Mutation	p.Pro544SerfsTer11(p.P544Sfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000448097
Start	7848307:7848308(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2025dupC
AA Mutation	p.Thr676HisfsTer8(p.T676Hfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KDM6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448097
Start	7849209:7849209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759948935
CDS Mutation	c.2921G>A
AA Mutation	p.Arg974Gln(p.R974Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript