Colon Cancer: Gene >> KDM3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138399931:138399931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3118A>G
AA Mutation	p.Asn1040Asp(p.N1040D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138420901:138420901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3911T>A
AA Mutation	p.Leu1304His(p.L1304H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138377777:138377777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>T
AA Mutation	p.Val178Phe(p.V178F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391077:138391077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445C>A
AA Mutation	p.Pro482His(p.P482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391421:138391421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789T>A
AA Mutation	p.Ser597Thr(p.S597T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138420919:138420919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3929A>G
AA Mutation	p.Asp1310Gly(p.D1310G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138429880:138429880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4808T>G
AA Mutation	p.Ile1603Ser(p.I1603S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391121:138391121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489G>A
AA Mutation	p.Ala497Thr(p.A497T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138381532:138381532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722C>T
AA Mutation	p.Ser241Leu(p.S241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000314358
Start	138420960:138420960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3970G>C
AA Mutation	p.Ala1324Pro(p.A1324P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138386094:138386094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Trp(p.R285W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000314358
Start	138381588:138381588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Glu260Lys(p.E260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138400006:138400006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539384678
CDS Mutation	c.3193C>T
AA Mutation	p.Arg1065Cys(p.R1065C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138427236:138427236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4550G>A
AA Mutation	p.Arg1517Gln(p.R1517Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138393230:138393230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2689C>T
AA Mutation	p.Pro897Ser(p.P897S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391079:138391079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447T>G
AA Mutation	p.Leu483Val(p.L483V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138430333:138430333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4978A>G
AA Mutation	p.Lys1660Glu(p.K1660E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391186:138391186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554C>A
AA Mutation	p.Asp518Glu(p.D518E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138393358:138393358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2817C>A
AA Mutation	p.Phe939Leu(p.F939L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138391954:138391954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140375150
CDS Mutation	c.2322C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138427312:138427312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368913432
CDS Mutation	c.4626C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138424314:138424314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4212C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138425569:138425569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762393674
CDS Mutation	c.4398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314358
Start	138391505:138391505(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1878delC
AA Mutation	p.Lys627AsnfsTer60(p.K627Nfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314358
Start	138420936:138420936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3950delC
AA Mutation	p.Pro1317ArgfsTer10(p.P1317Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138392036:138392036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2404C>T
AA Mutation	p.Arg802Ter(p.R802*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138417560:138417560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3385C>T
AA Mutation	p.Arg1129Ter(p.R1129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138377822:138377822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Ter(p.R193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138386202:138386202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Ter(p.R321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000314358
Start	138398393:138398393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3046+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KDM3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138393339:138393339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2798C>T
AA Mutation	p.Ser933Phe(p.S933F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391297:138391297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665C>G
AA Mutation	p.Asp555Glu(p.D555E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391241:138391241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609A>C
AA Mutation	p.Ser537Arg(p.S537R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138430330:138430330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4975C>T
AA Mutation	p.Arg1659Cys(p.R1659C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138386183:138386183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138372812:138372812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Ter(p.R111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript