Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> JMJD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76725746:76725746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>A
AA Mutation	p.Ser80Tyr(p.S80Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76723853:76723853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374399276
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Trp(p.R242W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76718805:76718805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377582812
CDS Mutation	c.1136C>T
AA Mutation	p.Thr379Met(p.T379M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76725804:76725804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>A
AA Mutation	p.Glu61Lys(p.E61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76726429:76726429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47C>T
AA Mutation	p.Ala16Val(p.A16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76725781:76725781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>T
AA Mutation	p.Lys68Asn(p.K68N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> JMJD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76725522:76725522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463T>A
AA Mutation	p.Phe155Ile(p.F155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397625
Start	76726448:76726448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28C>G
AA Mutation	p.Arg10Gly(p.R10G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397625
Start	76725540:76725541(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.444dupA
AA Mutation	p.Asp149ArgfsTer10(p.D149Rfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript