Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF131

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000509156
Start	43161482:43161482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757762026
CDS Mutation	c.605G>A
AA Mutation	p.Ser202Asn(p.S202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000509156
Start	43161769:43161769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892C>A
AA Mutation	p.Leu298Ile(p.L298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000509156
Start	43123232:43123232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>A
AA Mutation	p.Ala50Thr(p.A50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000509156
Start	43161304:43161304(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.433delA
AA Mutation	p.Arg145GlyfsTer26(p.R145Gfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000509156
Start	43173415:43173415(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1158delA
AA Mutation	p.Gly387GlufsTer26(p.G387Efs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000509156
Start	43161877:43161877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>T
AA Mutation	p.Glu334Ter(p.E334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF131

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000509156
Start	43161251:43161251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374A>G
AA Mutation	p.Asn125Ser(p.N125S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000509156
Start	43174624:43174624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363C>A
AA Mutation	p.Leu455Ile(p.L455I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000509156
Start	43123228:43123228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000509156
Start	43161304:43161304(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.433delA
AA Mutation	p.Arg145GlyfsTer26(p.R145Gfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript