Mutation

Primary Site >> Stomach Cancer

Gene >> JMJD1C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63207800:63207800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3869A>G
AA Mutation	p.His1290Arg(p.H1290R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63207504:63207504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4165A>G
AA Mutation	p.Asn1389Asp(p.N1389D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63214903:63214903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>A
AA Mutation	p.Ala422Thr(p.A422T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63214047:63214047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2120A>C
AA Mutation	p.Lys707Thr(p.K707T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63213477:63213477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2690G>T
AA Mutation	p.Arg897Met(p.R897M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63215675:63215675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700G>A
AA Mutation	p.Asp234Asn(p.D234N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63176392:63176392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7306C>T
AA Mutation	p.Arg2436Cys(p.R2436C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63177820:63177820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7121A>G
AA Mutation	p.Asp2374Gly(p.D2374G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63184641:63184641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6928C>T
AA Mutation	p.Pro2310Ser(p.P2310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63207110:63207110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4559G>A
AA Mutation	p.Ser1520Asn(p.S1520N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63219931:63219931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500A>G
AA Mutation	p.Glu167Gly(p.E167G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63198569:63198569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5435A>C
AA Mutation	p.Lys1812Thr(p.K1812T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63194328:63194328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5692G>A
AA Mutation	p.Asp1898Asn(p.D1898N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63214849:63214849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>A
AA Mutation	p.Asp440Asn(p.D440N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63200480:63200480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5272A>G
AA Mutation	p.Arg1758Gly(p.R1758G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63207174:63207174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4495G>A
AA Mutation	p.Ala1499Thr(p.A1499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63380428:63380428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190890554
CDS Mutation	c.223T>C
AA Mutation	p.Tyr75His(p.Y75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63198696:63198696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5308A>G
AA Mutation	p.Ile1770Val(p.I1770V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63184646:63184646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6923T>C
AA Mutation	p.Val2308Ala(p.V2308A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000399262
Start	63207489:63207489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4180A>G
AA Mutation	p.Thr1394Ala(p.T1394A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63200652:63200652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5100A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63200493:63200493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5259A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63198574:63198574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5430T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63191005:63191005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6180T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63193050:63193050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5964C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63209140:63209140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2790A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63183547:63183547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6984T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63207979:63207979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3690A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63207151:63207151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4518T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63189429:63189429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6309G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399262
Start	63219968:63219968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63214881:63214881(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1286delA
AA Mutation	p.Asn429IlefsTer32(p.N429Ifs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000399262
Start	63192939:63192939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6075delA
AA Mutation	p.Glu2026LysfsTer45(p.E2026Kfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63207218:63207218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4451delA
AA Mutation	p.Lys1484SerfsTer24(p.K1484Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63200529:63200529(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5223delA
AA Mutation	p.Gly1742GlufsTer26(p.G1742Efs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63208739:63208739(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2930delA
AA Mutation	p.Asn977MetfsTer5(p.N977Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63214490:63214490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1677delA
AA Mutation	p.Asp560IlefsTer10(p.D560Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63207143:63207143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4526delA
AA Mutation	p.Asn1509IlefsTer14(p.N1509Ifs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63198710:63198710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5294delA
AA Mutation	p.Asn1765ThrfsTer3(p.N1765Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000399262
Start	63192938:63192939(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.6075dupA
AA Mutation	p.Glu2026ArgfsTer8(p.E2026Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399262
Start	63207142:63207143(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4526dupA
AA Mutation	p.Asn1509LysfsTer12(p.N1509Kfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript