Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZBED8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394226:160394226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1265G>T
AA Mutation	p.Arg422Ile(p.R422I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394530:160394530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961G>A
AA Mutation	p.Glu321Lys(p.E321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394840:160394840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748101427
CDS Mutation	c.651A>G
AA Mutation	p.Ile217Met(p.I217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394922:160394922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569C>T
AA Mutation	p.Ala190Val(p.A190V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394433:160394433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058T>A
AA Mutation	p.Phe353Tyr(p.F353Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394731:160394731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371131252
CDS Mutation	c.760G>A
AA Mutation	p.Glu254Lys(p.E254K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160395376:160395376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115A>G
AA Mutation	p.Asn39Asp(p.N39D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000408953
Start	160395087:160395087(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.404delA
AA Mutation	p.Lys135SerfsTer11(p.K135Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000408953
Start	160393766:160393766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1725delA
AA Mutation	p.Val576PhefsTer28(p.V576Ffs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBED8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160395277:160395277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214C>T
AA Mutation	p.Pro72Ser(p.P72S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394431:160394431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060C>A
AA Mutation	p.Leu354Ile(p.L354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394705:160394705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786G>T
AA Mutation	p.Glu262Asp(p.E262D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000408953
Start	160394920:160394920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571T>C
AA Mutation	p.Phe191Leu(p.F191L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408953
Start	160394678:160394678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408953
Start	160395053:160395053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408953
Start	160394891:160394891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373610961
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript