Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KDM4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335080
Start	94998849:94998849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477G>C
AA Mutation	p.Glu493Gln(p.E493Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335080
Start	94997503:94997503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131A>C
AA Mutation	p.His44Pro(p.H44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335080
Start	94998186:94998186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814A>G
AA Mutation	p.Met272Val(p.M272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335080
Start	94998143:94998143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771T>G
AA Mutation	p.Asn257Lys(p.N257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335080
Start	94997558:94997558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335080
Start	94997643:94997643(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs142280183
CDS Mutation	c.278delA
AA Mutation	p.Lys93ArgfsTer4(p.K93Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335080
Start	94997642:94997643(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.278dupA
AA Mutation	p.Lys94GlufsTer15(p.K94Efs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KDM4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335080
Start	94998735:94998735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782590036
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Cys(p.R455C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335080
Start	94998344:94998344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript