Mutation

Primary Site >> Stomach Cancer

Gene >> DISP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40369369:40369369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779760492
CDS Mutation	c.3257G>A
AA Mutation	p.Arg1086His(p.R1086H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367332:40367332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220C>T
AA Mutation	p.Ala407Val(p.A407V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40368943:40368943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944His(p.R944H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40365155:40365155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728C>T
AA Mutation	p.Ser243Phe(p.S243F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40369717:40369717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199820901
CDS Mutation	c.3605C>T
AA Mutation	p.Pro1202Leu(p.P1202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367409:40367409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297C>T
AA Mutation	p.Leu433Phe(p.L433F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40364516:40364516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>T
AA Mutation	p.Arg192Leu(p.R192L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40369194:40369194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3082C>A
AA Mutation	p.Leu1028Ile(p.L1028I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367424:40367424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370777054
CDS Mutation	c.1312C>T
AA Mutation	p.Leu438Phe(p.L438F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367328:40367328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216A>G
AA Mutation	p.Ser406Gly(p.S406G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40369263:40369263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763352261
CDS Mutation	c.3151C>T
AA Mutation	p.Arg1051Cys(p.R1051C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367635:40367635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508His(p.R508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40367634:40367634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522C>T
AA Mutation	p.Arg508Cys(p.R508C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40368928:40368928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2816C>A
AA Mutation	p.Pro939His(p.P939H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267889
Start	40369651:40369651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3539C>A
AA Mutation	p.Thr1180Lys(p.T1180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267889
Start	40368911:40368911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140286504
CDS Mutation	c.2799G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267889
Start	40367114:40367114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267889
Start	40364238:40364238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267889
Start	40363814:40363814(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.314delG
AA Mutation	p.Gly105AlafsTer60(p.G105Afs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267889
Start	40368720:40368720(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2612delT
AA Mutation	p.Phe871SerfsTer5(p.F871Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267889
Start	40367485:40367485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1377delC
AA Mutation	p.Trp460GlyfsTer22(p.W460Gfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000267889
Start	40367126:40367127(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1014_1015insAATCATGTAGTGTGATGACTTA
AA Mutation	p.Ser339AsnfsTer5(p.S339Nfs*5)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000267889
Start	40364224:40364224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript