Mutation

Primary Site >> Stomach Cancer

Gene >> KDM5C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53217911:53217911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53224850:53224850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40T>A
AA Mutation	p.Cys14Ser(p.C14S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53196819:53196819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2848A>G
AA Mutation	p.Met950Val(p.M950V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53201710:53201710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1901G>A
AA Mutation	p.Arg634His(p.R634H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53218385:53218385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242T>C
AA Mutation	p.Val81Ala(p.V81A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53217169:53217169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Trp(p.R211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53201604:53201604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2007G>C
AA Mutation	p.Glu669Asp(p.E669D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53192998:53192998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4652G>A
AA Mutation	p.Cys1551Tyr(p.C1551Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53210735:53210735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524C>G
AA Mutation	p.Phe508Leu(p.F508L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53193224:53193224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4426G>A
AA Mutation	p.Glu1476Lys(p.E1476K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53193161:53193161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4489G>C
AA Mutation	p.Glu1497Gln(p.E1497Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53210820:53210820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439C>A
AA Mutation	p.Pro480Gln(p.P480Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53198590:53198590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416T>C
AA Mutation	p.Phe806Leu(p.F806L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53217831:53217831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487C>T
AA Mutation	p.Pro163Ser(p.P163S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000375401
Start	53217842:53217842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476G>A
AA Mutation	p.Arg159His(p.R159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53198870:53198870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2262T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53211811:53211811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53201884:53201884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373804164
CDS Mutation	c.1836C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53215801:53215801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53211895:53211895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53193490:53193490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4264C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53211826:53211826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782716338
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53215897:53215897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61751238
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375401
Start	53198531:53198531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375401
Start	53193127:53193127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4523delC
AA Mutation	p.Pro1508LeufsTer36(p.P1508Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375401
Start	53217211:53217211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.589delC
AA Mutation	p.Leu197TyrfsTer37(p.L197Yfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375401
Start	53201925:53201925(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1795delC
AA Mutation	p.Arg599ValfsTer60(p.R599Vfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375401
Start	53193126:53193127(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4523dupC
AA Mutation	p.Ala1509CysfsTer75(p.A1509Cfs*75)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375401
Start	53198855:53198856(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2276dupT
AA Mutation	p.Met759IlefsTer4(p.M759Ifs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000375401
Start	53195914:53195914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3120+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript