Mutation

Primary Site >> Stomach Cancer

Gene >> DNMT3B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32792740:32792740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>A
AA Mutation	p.Glu346Lys(p.E346K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32798578:32798578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771223602
CDS Mutation	c.1609C>T
AA Mutation	p.Arg537Trp(p.R537W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32799286:32799286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764722946
CDS Mutation	c.1717C>T
AA Mutation	p.Arg573Trp(p.R573W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32800197:32800197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752495145
CDS Mutation	c.1804G>A
AA Mutation	p.Val602Ile(p.V602I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32799281:32799281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778795266
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571Gln(p.R571Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32792707:32792707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003T>C
AA Mutation	p.Trp335Arg(p.W335R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32801416:32801416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2135G>A
AA Mutation	p.Arg712Gln(p.R712Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32798546:32798546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1577T>G
AA Mutation	p.Met526Arg(p.M526R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32801367:32801367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2086T>C
AA Mutation	p.Phe696Leu(p.F696L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32799323:32799323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754C>T
AA Mutation	p.Ala585Val(p.A585V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32784842:32784842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769220144
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32795475:32795475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751976489
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398His(p.R398H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32798603:32798603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572676072
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545His(p.R545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32787313:32787313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202113400
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32798508:32798508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772289824
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32800909:32800909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32806250:32806250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2343C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32799273:32799273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766064158
CDS Mutation	c.1704C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32780425:32780425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564154904
CDS Mutation	c.102G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32788919:32788919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328111
Start	32796845:32796845(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1359delG
AA Mutation	p.Leu454SerfsTer136(p.L454Sfs*136)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328111
Start	32787354:32787354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.561delC
AA Mutation	p.Tyr188ThrfsTer4(p.Y188Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32807859:32807859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518C>T
AA Mutation	p.Arg840Ter(p.R840*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32792638:32792638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Ter(p.R312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32799295:32799295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726C>T
AA Mutation	p.Arg576Ter(p.R576*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript