Colon Cancer: Gene >> ZBTB16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114064148:114064148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>T
AA Mutation	p.Pro283Leu(p.P283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114064400:114064400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100A>C
AA Mutation	p.Asp367Ala(p.D367A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114156404:114156404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>T
AA Mutation	p.Arg446Trp(p.R446W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114064381:114064381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750494052
CDS Mutation	c.1081G>T
AA Mutation	p.Ala361Ser(p.A361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114250349:114250349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1816C>G
AA Mutation	p.Leu606Val(p.L606V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114156368:114156368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300T>A
AA Mutation	p.Cys434Ser(p.C434S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114063572:114063572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>T
AA Mutation	p.Thr91Met(p.T91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335953
Start	114186952:114186952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367C>T
AA Mutation	p.Ala456Val(p.A456V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114247223:114247223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650C>A
AA Mutation	p.Phe550Leu(p.F550L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114156365:114156365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538741723
CDS Mutation	c.1297G>A
AA Mutation	p.Gly433Arg(p.G433R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114250403:114250403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870C>T
AA Mutation	p.His624Tyr(p.H624Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114063646:114063646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>A
AA Mutation	p.Glu116Lys(p.E116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114063557:114063557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257A>G
AA Mutation	p.Tyr86Cys(p.Y86C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114242205:114242205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Cys(p.R498C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114247301:114247301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114064347:114064347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200705288
CDS Mutation	c.1047G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114064278:114064278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760505512
CDS Mutation	c.978G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114063477:114063477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114186983:114186983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116547293
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114247346:114247346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778496413
CDS Mutation	c.1773G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114250531:114250531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335953
Start	114063312:114063312(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.16delA
AA Mutation	p.Met6TrpfsTer3(p.M6Wfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335953
Start	114242197:114242198(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1485dupT
AA Mutation	p.Gly496TrpfsTer27(p.G496Wfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000335953
Start	114187021:114187022(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1436_1437insACTGTG
AA Mutation	p.His479delinsGlnLeuCys(p.H479delinsQLC)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114242205:114242205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Cys(p.R498C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114063572:114063572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>T
AA Mutation	p.Thr91Met(p.T91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335953
Start	114186997:114186997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761753131
CDS Mutation	c.1412C>T
AA Mutation	p.Ser471Leu(p.S471L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335953
Start	114242234:114242234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753894958
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000335953
Start	114064153:114064153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Ter(p.R285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript