Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DCAF4L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873192:87873192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>G
AA Mutation	p.Ser260Arg(p.S260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873458:87873458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780981376
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87872815:87872815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873754:87873754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873944:87873944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768880591
CDS Mutation	c.28G>A
AA Mutation	p.Glu10Lys(p.E10K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873586:87873586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>A
AA Mutation	p.Ser129Tyr(p.S129Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873454:87873454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Arg173Gln(p.R173Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873212:87873212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>T
AA Mutation	p.Arg254Cys(p.R254C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873490:87873490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367683322
CDS Mutation	c.482C>T
AA Mutation	p.Ala161Val(p.A161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87872959:87872959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Thr338Met(p.T338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87872978:87872978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747432904
CDS Mutation	c.994G>A
AA Mutation	p.Val332Met(p.V332M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873900:87873900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72T>A
AA Mutation	p.Asn24Lys(p.N24K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873676:87873676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.296A>G
AA Mutation	p.Tyr99Cys(p.Y99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873824:87873824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Cys(p.R50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873175:87873175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>A
AA Mutation	p.Cys266Tyr(p.C266Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873154:87873154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818T>C
AA Mutation	p.Val273Ala(p.V273A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873644:87873644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>A
AA Mutation	p.Pro110Thr(p.P110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873467:87873467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Pro169Ser(p.P169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873463:87873463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509G>T
AA Mutation	p.Gly170Val(p.G170V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873263:87873263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709C>T
AA Mutation	p.Pro237Ser(p.P237S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873211:87873211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>A
AA Mutation	p.Arg254His(p.R254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873679:87873679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293A>G
AA Mutation	p.Lys98Arg(p.K98R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873457:87873457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873829:87873829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143A>G
AA Mutation	p.Glu48Gly(p.E48G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873126:87873126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873489:87873489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873855:87873855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779092689
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87872889:87872889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141776325
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87872856:87872856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873426:87873426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873819:87873819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873735:87873735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873384:87873384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760989849
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87872973:87872973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000319675
Start	87873846:87873846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126T>A
AA Mutation	p.Tyr42Ter(p.Y42*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000319675
Start	87873659:87873659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200433622
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Ter(p.R105*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DCAF4L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87872956:87872956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>T
AA Mutation	p.Arg339Ile(p.R339I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873586:87873586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>A
AA Mutation	p.Ser129Tyr(p.S129Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873080:87873080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>T
AA Mutation	p.Asp298Tyr(p.D298Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873223:87873223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749G>A
AA Mutation	p.Gly250Asp(p.G250D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87872959:87872959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Thr338Met(p.T338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873328:87873328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141897217
CDS Mutation	c.644C>T
AA Mutation	p.Thr215Met(p.T215M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319675
Start	87873241:87873241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731G>A
AA Mutation	p.Arg244His(p.R244H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873489:87873489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319675
Start	87873855:87873855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779092689
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000319675
Start	87873579:87873579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393C>A
AA Mutation	p.Cys131Ter(p.C131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript