Mutation

Primary Site >> Stomach Cancer

Gene >> KDM5B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202749025:202749025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769638696
CDS Mutation	c.1936G>A
AA Mutation	p.Val646Ile(p.V646I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202764091:202764091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766C>G
AA Mutation	p.Leu256Val(p.L256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202741529:202741529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2783T>C
AA Mutation	p.Leu928Pro(p.L928P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202730989:202730989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4096C>T
AA Mutation	p.Leu1366Phe(p.L1366F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202733712:202733712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3598C>A
AA Mutation	p.His1200Asn(p.H1200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202741560:202741560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2752C>T
AA Mutation	p.Arg918Cys(p.R918C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202745971:202745971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2210C>T
AA Mutation	p.Thr737Met(p.T737M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202735476:202735476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3376A>G
AA Mutation	p.Ser1126Gly(p.S1126G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202733552:202733552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758565397
CDS Mutation	c.3758G>A
AA Mutation	p.Arg1253Gln(p.R1253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202741493:202741493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368783569
CDS Mutation	c.2819G>A
AA Mutation	p.Arg940His(p.R940H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202741538:202741538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2774A>C
AA Mutation	p.Gln925Pro(p.Q925P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202729043:202729043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761912360
CDS Mutation	c.4628G>A
AA Mutation	p.Arg1543Gln(p.R1543Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202736383:202736383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746793440
CDS Mutation	c.3094C>T
AA Mutation	p.Arg1032Cys(p.R1032C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202777042:202777042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257G>A
AA Mutation	p.Arg86His(p.R86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202741661:202741661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781211319
CDS Mutation	c.2651C>T
AA Mutation	p.Thr884Met(p.T884M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367265
Start	202733610:202733610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3700C>T
AA Mutation	p.Pro1234Ser(p.P1234S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202752977:202752977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202729123:202729123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4548C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202755318:202755318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202730951:202730951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4134G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202733683:202733683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3627T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202735584:202735584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367265
Start	202777047:202777047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760438429
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367265
Start	202735497:202735497(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3355delA
AA Mutation	p.Ser1119AlafsTer4(p.S1119Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367265
Start	202729875:202729875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4329delC
AA Mutation	p.Lys1444ArgfsTer3(p.K1444Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000367265
Start	202742450:202742450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530C>T
AA Mutation	p.Gln844Ter(p.Q844*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000367265
Start	202740676:202740676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3082C>T
AA Mutation	p.Gln1028Ter(p.Q1028*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000367265
Start	202746324:202746324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript