Mutation

Primary Site >> Stomach Cancer

Gene >> KDM5A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	310979:310979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564426386
CDS Mutation	c.3122C>T
AA Mutation	p.Pro1041Leu(p.P1041L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	333525:333525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1615A>G
AA Mutation	p.Ile539Val(p.I539V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	328984:328984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1819C>T
AA Mutation	p.Arg607Cys(p.R607C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	323611:323611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139G>T
AA Mutation	p.Lys713Asn(p.K713N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	307603:307603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773466573
CDS Mutation	c.3781C>T
AA Mutation	p.Arg1261Trp(p.R1261W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	311009:311009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3092G>A
AA Mutation	p.Arg1031His(p.R1031H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	352233:352233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121A>G
AA Mutation	p.Lys374Arg(p.K374R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	334325:334325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406C>A
AA Mutation	p.Pro469Gln(p.P469Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	323652:323652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2098C>T
AA Mutation	p.Leu700Phe(p.L700F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	356522:356522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>C
AA Mutation	p.Val230Leu(p.V230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	307626:307626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3758C>T
AA Mutation	p.Ala1253Val(p.A1253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	334385:334385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>T
AA Mutation	p.Pro449Leu(p.P449L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	323664:323664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2086C>T
AA Mutation	p.Arg696Trp(p.R696W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	318439:318439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2564A>T
AA Mutation	p.Glu855Val(p.E855V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399788
Start	307486:307486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3898C>T
AA Mutation	p.Leu1300Phe(p.L1300F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	313188:313188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2904G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	318321:318321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2682G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	389041:389041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	318288:318288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747419006
CDS Mutation	c.2715C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	323182:323182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752225628
CDS Mutation	c.2175C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399788
Start	307823:307823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399788
Start	389069:389069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.23delG
AA Mutation	p.Gly8AlafsTer58(p.G8Afs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399788
Start	307787:307787(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774964135
CDS Mutation	c.3597delA
AA Mutation	p.Gly1200AspfsTer9(p.G1200Dfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000399788
Start	323083:323083(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2274delA
AA Mutation	p.Asp759IlefsTer2(p.D759Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399788
Start	309905:309905(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3276delA
AA Mutation	p.Val1093Ter(p.V1093*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000399788
Start	355238:355238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Ter(p.R264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000399788
Start	321063:321063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2473G>T
AA Mutation	p.Glu825Ter(p.E825*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000399788
Start	310942:310942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3159G>A
AA Mutation	p.Trp1053Ter(p.W1053*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000399788
Start	355156:355156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript