Mutation

Primary Site >> Stomach Cancer

Gene >> DNMT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10140837:10140837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767421908
CDS Mutation	c.3419G>A
AA Mutation	p.Arg1140Gln(p.R1140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10149508:10149508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2483T>C
AA Mutation	p.Ile828Thr(p.I828T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10159910:10159910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054A>G
AA Mutation	p.Lys352Glu(p.K352E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10148969:10148969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2587T>C
AA Mutation	p.Tyr863His(p.Y863H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10156496:10156496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181300723
CDS Mutation	c.1246C>T
AA Mutation	p.His416Tyr(p.H416Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10180479:10180479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759600542
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10148999:10148999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2557T>C
AA Mutation	p.Ser853Pro(p.S853P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10156460:10156460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Glu428Lys(p.E428K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10138590:10138590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3916G>A
AA Mutation	p.Val1306Met(p.V1306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10140237:10140237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3567G>T
AA Mutation	p.Glu1189Asp(p.E1189D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000340748
Start	10149853:10149853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2333G>T
AA Mutation	p.Arg778Met(p.R778M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10146477:10146477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2720T>C
AA Mutation	p.Ile907Thr(p.I907T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10140113:10140113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3691G>T
AA Mutation	p.Gly1231Cys(p.G1231C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10151426:10151426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2189G>A
AA Mutation	p.Arg730His(p.R730H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10140103:10140103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3701G>A
AA Mutation	p.Arg1234His(p.R1234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10137945:10137945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4132C>T
AA Mutation	p.Arg1378Trp(p.R1378W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10142201:10142201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3088T>C
AA Mutation	p.Ser1030Pro(p.S1030P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10142180:10142180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370786558
CDS Mutation	c.3109G>A
AA Mutation	p.Ala1037Thr(p.A1037T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10138510:10138510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751126457
CDS Mutation	c.3996C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10166634:10166634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755151805
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10137961:10137961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779701784
CDS Mutation	c.4116C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10154768:10154768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10140065:10140065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3739C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340748
Start	10160391:10160392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.987dupC
AA Mutation	p.Lys330GlnfsTer35(p.K330Qfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript