Mutation

Primary Site >> Stomach Cancer

Gene >> KDM4C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7015923:7015923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2253G>C
AA Mutation	p.Trp751Cys(p.W751C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6805761:6805761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>T
AA Mutation	p.Ala103Ser(p.A103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7169838:7169838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2942A>T
AA Mutation	p.Glu981Val(p.E981V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6793019:6793019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31A>G
AA Mutation	p.Asn11Asp(p.N11D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7013971:7013971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2152T>C
AA Mutation	p.Cys718Arg(p.C718R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6805671:6805671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217A>G
AA Mutation	p.Ile73Val(p.I73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7103815:7103815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2555A>G
AA Mutation	p.Asp852Gly(p.D852G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6805770:6805770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Gly106Ser(p.G106S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6814672:6814672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780836880
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7128217:7128217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753394685
CDS Mutation	c.2762C>T
AA Mutation	p.Thr921Ile(p.T921I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6984274:6984274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224T>G
AA Mutation	p.Asp408Glu(p.D408E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	7013988:7013988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2169A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	6986411:6986411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	7015920:7015920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774249515
CDS Mutation	c.2250G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	6888045:6888045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35244873
CDS Mutation	c.765T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	7174666:7174666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145856633
CDS Mutation	c.3108C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381309
Start	7103861:7103861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2604delC
AA Mutation	p.Asn869ThrfsTer2(p.N869Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381309
Start	7011795:7011795(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1884delC
AA Mutation	p.Phe628LeufsTer14(p.F628Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000381309
Start	7174616:7174616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3058A>T
AA Mutation	p.Arg1020Ter(p.R1020*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript