Mutation

Primary Site >> Stomach Cancer

Gene >> SETD2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47097960:47097960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5137G>T
AA Mutation	p.Asp1713Tyr(p.D1713Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47121937:47121937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2699G>A
AA Mutation	p.Cys900Tyr(p.C900Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47120755:47120755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3881G>A
AA Mutation	p.Gly1294Asp(p.G1294D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47057390:47057390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769623377
CDS Mutation	c.6394C>T
AA Mutation	p.Arg2132Trp(p.R2132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47084379:47084379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5401A>G
AA Mutation	p.Ile1801Val(p.I1801V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47123017:47123017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371758386
CDS Mutation	c.1619G>A
AA Mutation	p.Arg540Gln(p.R540Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47062226:47062226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6230G>A
AA Mutation	p.Arg2077Gln(p.R2077Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47084234:47084234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5546C>T
AA Mutation	p.Ser1849Leu(p.S1849L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47121187:47121187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3449G>T
AA Mutation	p.Arg1150Ile(p.R1150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47084294:47084294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5486A>C
AA Mutation	p.Gln1829Pro(p.Q1829P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47122975:47122975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375514539
CDS Mutation	c.1661G>A
AA Mutation	p.Arg554His(p.R554H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47106061:47106061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4775G>A
AA Mutation	p.Arg1592Gln(p.R1592Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47113969:47113969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4622A>G
AA Mutation	p.Asn1541Ser(p.N1541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47121469:47121469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776300341
CDS Mutation	c.3167C>T
AA Mutation	p.Ser1056Leu(p.S1056L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000409792
Start	47057033:47057033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6751G>C
AA Mutation	p.Asp2251His(p.D2251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409792
Start	47057340:47057340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6444A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409792
Start	47046508:47046508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7077G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409792
Start	47057304:47057304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368137896
CDS Mutation	c.6480G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409792
Start	47122782:47122782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1854A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47042656:47042656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7143delC
AA Mutation	p.Ser2382LeufsTer29(p.S2382Lfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47062176:47062176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6280delA
AA Mutation	p.Arg2094GlyfsTer53(p.R2094Gfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47120417:47120417(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4219delA
AA Mutation	p.Arg1407GlyfsTer5(p.R1407Gfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000409792
Start	47086203:47086203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5389C>T
AA Mutation	p.Gln1797Ter(p.Q1797*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47120416:47120417(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4219dupA
AA Mutation	p.Arg1407LysfsTer8(p.R1407Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47062264:47062265(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749901643
CDS Mutation	c.6190_6191dupGA
AA Mutation	p.Asp2064GlufsTer84(p.D2064Efs*84)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409792
Start	47101519:47101520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4953dupT
AA Mutation	p.Thr1652TyrfsTer14(p.T1652Yfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000409792
Start	47101456:47101456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5015+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript