Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF165

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28088606:28088606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594T>G
AA Mutation	p.Ile198Met(p.I198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28089183:28089183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150379905
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Trp(p.R391W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28085790:28085790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Asp104Asn(p.D104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28085845:28085845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365C>T
AA Mutation	p.Thr122Ile(p.T122I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28089187:28089187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757188413
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392Gln(p.R392Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377325
Start	28088789:28088789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000377325
Start	28085556:28085556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76G>T
AA Mutation	p.Glu26Ter(p.E26*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF165

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28088921:28088921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909G>T
AA Mutation	p.Trp303Cys(p.W303C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28085566:28085566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86T>G
AA Mutation	p.Phe29Cys(p.F29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377325
Start	28086199:28086199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439A>C
AA Mutation	p.Ile147Leu(p.I147L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000377325
Start	28088730:28088730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718G>T
AA Mutation	p.Glu240Ter(p.E240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript