Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZBTB33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254006:120254006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591T>G
AA Mutation	p.Phe197Leu(p.F197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120255219:120255219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1804G>C
AA Mutation	p.Asp602His(p.D602H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120253961:120253961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546G>T
AA Mutation	p.Lys182Asn(p.K182N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254916:120254916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1501A>G
AA Mutation	p.Arg501Gly(p.R501G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254407:120254407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992A>C
AA Mutation	p.Glu331Ala(p.E331A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254080:120254080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665G>A
AA Mutation	p.Gly222Asp(p.G222D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254283:120254283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868A>G
AA Mutation	p.Thr290Ala(p.T290A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254788:120254788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373G>T
AA Mutation	p.Arg458Ile(p.R458I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120253462:120253462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Gly16Asp(p.G16D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120255370:120255370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1955T>A
AA Mutation	p.Ile652Asn(p.I652N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120255394:120255394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781978909
CDS Mutation	c.1979G>A
AA Mutation	p.Gly660Asp(p.G660D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120255387:120255387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972A>G
AA Mutation	p.Thr658Ala(p.T658A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254371:120254371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956C>T
AA Mutation	p.Ala319Val(p.A319V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120254862:120254862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447C>A
AA Mutation	p.His483Asn(p.H483N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254984:120254984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254354:120254354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17854233
CDS Mutation	c.939G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254345:120254345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254471:120254471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326624
Start	120254002:120254002(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.592delT
AA Mutation	p.Cys198AlafsTer43(p.C198Afs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326624
Start	120255103:120255103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1688A>G
AA Mutation	p.Gln563Arg(p.Q563R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254732:120254732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1317A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254417:120254417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326624
Start	120254726:120254726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript