Mutation

Primary Site >> Stomach Cancer

Gene >> KDM2B

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377071
Start	121580786:121580786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126G>T
AA Mutation	p.Gln42His(p.Q42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121442251:121442251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368157368
CDS Mutation	c.3190G>A
AA Mutation	p.Val1064Ile(p.V1064I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121430404:121430404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3895G>T
AA Mutation	p.Asp1299Tyr(p.D1299Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121444053:121444053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2410C>T
AA Mutation	p.Arg804Trp(p.R804W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121441147:121441147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3371G>A
AA Mutation	p.Arg1124Gln(p.R1124Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121509665:121509665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549C>A
AA Mutation	p.Leu517Met(p.L517M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121578909:121578909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164A>G
AA Mutation	p.Asp55Gly(p.D55G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121521005:121521005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Glu343Lys(p.E343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121442632:121442632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2809C>T
AA Mutation	p.Arg937Trp(p.R937W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121430356:121430356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3943A>G
AA Mutation	p.Ile1315Val(p.I1315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121521029:121521029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781923527
CDS Mutation	c.1003G>A
AA Mutation	p.Val335Met(p.V335M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121453157:121453157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922G>A
AA Mutation	p.Arg641His(p.R641H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377071
Start	121532937:121532937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>T
AA Mutation	p.Thr267Met(p.T267M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121453231:121453231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121444078:121444078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2385T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121440835:121440835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141490235
CDS Mutation	c.3591G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121532915:121532915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782547447
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121549556:121549556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782376095
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377071
Start	121521054:121521054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554683740
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121521064:121521065(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.967_968delTT
AA Mutation	p.Leu323GlyfsTer11(p.L323Gfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121442425:121442425(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3016delC
AA Mutation	p.Arg1006GlyfsTer37(p.R1006Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121580868:121580868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.44delC
AA Mutation	p.Pro15HisfsTer92(p.P15Hfs*92)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121580835:121580835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.77delA
AA Mutation	p.Lys26ArgfsTer81(p.K26Rfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121442478:121442478(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2963delC
AA Mutation	p.Pro988ArgfsTer55(p.P988Rfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000377071
Start	121453245:121453245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1834C>T
AA Mutation	p.Arg612Ter(p.R612*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377071
Start	121442288:121442289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3152dupC
AA Mutation	p.Pro1052AlafsTer2(p.P1052Afs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000377071
Start	121578948:121578948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript