Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF277

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112342676:112342676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300T>G
AA Mutation	p.Ser434Ala(p.S434A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112286990:112286990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755559466
CDS Mutation	c.209C>T
AA Mutation	p.Ala70Val(p.A70V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112296247:112296247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401T>A
AA Mutation	p.Phe134Tyr(p.F134Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112342647:112342647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271A>G
AA Mutation	p.Glu424Gly(p.E424G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112337762:112337762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902C>A
AA Mutation	p.Ser301Tyr(p.S301Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361822
Start	112296260:112296260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142208106
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361822
Start	112330148:112330148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749826488
CDS Mutation	c.738delA
AA Mutation	p.Lys246AsnfsTer87(p.K246Nfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF277

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361822
Start	112342706:112342706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330A>G
AA Mutation	p.Ile444Val(p.I444V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361822
Start	112339851:112339851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150018093
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000361822
Start	112330184:112330184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>T
AA Mutation	p.Glu257Ter(p.E257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript