Mutation

Primary Site >> Stomach Cancer

Gene >> KDM4B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5047614:5047614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Glu191Lys(p.E191K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5032921:5032921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>A
AA Mutation	p.Pro11Thr(p.P11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5110661:5110661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749807599
CDS Mutation	c.958G>A
AA Mutation	p.Val320Met(p.V320M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5032909:5032909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756754407
CDS Mutation	c.19G>A
AA Mutation	p.Gly7Ser(p.G7S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5047492:5047492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>G
AA Mutation	p.Asn150Ser(p.N150S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5047629:5047629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586T>C
AA Mutation	p.Tyr196His(p.Y196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5071048:5071048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665G>A
AA Mutation	p.Arg222Gln(p.R222Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5119675:5119675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>T
AA Mutation	p.Pro380Ser(p.P380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5144096:5144096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2680G>A
AA Mutation	p.Asp894Asn(p.D894N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5144266:5144266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762143895
CDS Mutation	c.2755G>A
AA Mutation	p.Val919Met(p.V919M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5143988:5143988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553426005
CDS Mutation	c.2572C>T
AA Mutation	p.Arg858Trp(p.R858W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5131223:5131223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756397144
CDS Mutation	c.1463C>T
AA Mutation	p.Pro488Leu(p.P488L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5110739:5110739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754451824
CDS Mutation	c.1036C>T
AA Mutation	p.Arg346Trp(p.R346W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000159111
Start	5110814:5110814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Cys(p.R371C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5144068:5144068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2652C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5039886:5039886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753456068
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5077386:5077386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200324591
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5110648:5110648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5039982:5039982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5033001:5033001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200547114
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5133968:5133968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5135467:5135467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2214G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000159111
Start	5134040:5134040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159111
Start	5144140:5144140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2729delG
AA Mutation	p.Gly910ValfsTer7(p.G910Vfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000159111
Start	5131288:5131288(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1532delC
AA Mutation	p.Pro511LeufsTer8(p.P511Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript