Mutation

Primary Site >> Stomach Cancer

Gene >> KDM3B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391401:138391401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1769A>C
AA Mutation	p.Asp590Ala(p.D590A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138379682:138379682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138393354:138393354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2813G>A
AA Mutation	p.Arg938His(p.R938H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391746:138391746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2114T>G
AA Mutation	p.Val705Gly(p.V705G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138400001:138400001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758977082
CDS Mutation	c.3188G>A
AA Mutation	p.Arg1063Gln(p.R1063Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138398206:138398206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2860C>T
AA Mutation	p.Arg954Cys(p.R954C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391803:138391803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2171G>A
AA Mutation	p.Arg724His(p.R724H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000314358
Start	138379586:138379586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Pro195Ser(p.P195S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138435654:138435654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5240C>T
AA Mutation	p.Ala1747Val(p.A1747V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138427286:138427286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4600C>T
AA Mutation	p.Pro1534Ser(p.P1534S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138429868:138429868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4796C>T
AA Mutation	p.Thr1599Met(p.T1599M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138398359:138398359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3013G>C
AA Mutation	p.Glu1005Gln(p.E1005Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138393333:138393333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2792A>G
AA Mutation	p.Asp931Gly(p.D931G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138426991:138426991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4428A>C
AA Mutation	p.Glu1476Asp(p.E1476D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138399971:138399971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3158G>A
AA Mutation	p.Cys1053Tyr(p.C1053Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000314358
Start	138381588:138381588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Glu260Lys(p.E260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000314358
Start	138391389:138391389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757G>T
AA Mutation	p.Gly586Val(p.G586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138386504:138386504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1263A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138420941:138420941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144228142
CDS Mutation	c.3951G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138381587:138381587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367814427
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138386615:138386615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138377800:138377800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314358
Start	138372790:138372790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779436763
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314358
Start	138420936:138420936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3950delC
AA Mutation	p.Pro1317ArgfsTer10(p.P1317Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314358
Start	138430275:138430275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4925delC
AA Mutation	p.Pro1642LeufsTer36(p.P1642Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000314358
Start	138391901:138391901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2269C>T
AA Mutation	p.Gln757Ter(p.Q757*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript