Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF132

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433707:58433707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737C>A
AA Mutation	p.Phe579Leu(p.F579L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434206:58434206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1238G>A
AA Mutation	p.Ser413Asn(p.S413N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433562:58433562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758286151
CDS Mutation	c.1882G>A
AA Mutation	p.Glu628Lys(p.E628K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434599:58434599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845A>C
AA Mutation	p.Lys282Thr(p.K282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434570:58434570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>A
AA Mutation	p.Val292Met(p.V292M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434263:58434263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181A>G
AA Mutation	p.Gln394Arg(p.Q394R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434029:58434029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415C>G
AA Mutation	p.Ser472Cys(p.S472C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58437107:58437107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Ala58Thr(p.A58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434755:58434755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689G>A
AA Mutation	p.Cys230Tyr(p.C230Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433444:58433444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000G>T
AA Mutation	p.Arg667Ile(p.R667I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254166
Start	58433815:58433815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199698210
CDS Mutation	c.1629C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254166
Start	58434082:58434082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147170511
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254166
Start	58433851:58433851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254166
Start	58434913:58434913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150467107
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000254166
Start	58434393:58434393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051G>T
AA Mutation	p.Glu351Ter(p.E351*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF132

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433707:58433707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737C>A
AA Mutation	p.Phe579Leu(p.F579L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433889:58433889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781624681
CDS Mutation	c.1555G>A
AA Mutation	p.Glu519Lys(p.E519K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434619:58434619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>T
AA Mutation	p.Glu275Asp(p.E275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58434677:58434677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>T
AA Mutation	p.Arg256Ile(p.R256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254166
Start	58433562:58433562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758286151
CDS Mutation	c.1882G>A
AA Mutation	p.Glu628Lys(p.E628K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254166
Start	58433911:58433911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533G>A
Mutation Classification	Silent
Feature Type	Transcript