Mutation

Primary Site >> Stomach Cancer

Gene >> LMO7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75823739:75823739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2116T>C
AA Mutation	p.Ser706Pro(p.S706P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75842876:75842876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3358A>G
AA Mutation	p.Lys1120Glu(p.K1120E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841931:75841931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144089219
CDS Mutation	c.3280C>T
AA Mutation	p.Arg1094Cys(p.R1094C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75819414:75819414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749357751
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75804490:75804490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>T
AA Mutation	p.Arg55Ile(p.R55I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75808163:75808163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181G>A
AA Mutation	p.Ser394Asn(p.S394N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834337:75834337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2477C>T
AA Mutation	p.Ala826Val(p.A826V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834289:75834289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761122156
CDS Mutation	c.2429A>G
AA Mutation	p.Lys810Arg(p.K810R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75804391:75804391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375314137
CDS Mutation	c.65C>T
AA Mutation	p.Ala22Val(p.A22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75857927:75857927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4072G>A
AA Mutation	p.Gly1358Ser(p.G1358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000465261
Start	75842852:75842852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3334C>A
AA Mutation	p.Pro1112Thr(p.P1112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75823655:75823655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370412695
CDS Mutation	c.2032G>A
AA Mutation	p.Ala678Thr(p.A678T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75805618:75805618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760920054
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Cys(p.R119C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834373:75834373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747794496
CDS Mutation	c.2513G>A
AA Mutation	p.Arg838His(p.R838H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75857926:75857926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199772213
CDS Mutation	c.4071C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75807909:75807909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779966190
CDS Mutation	c.927T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75804479:75804479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75823654:75823654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377226161
CDS Mutation	c.2031C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75807654:75807654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75808029:75808029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75853257:75853257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3831C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75853251:75853251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3825G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75833116:75833116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465261
Start	75819419:75819419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs34219193
CDS Mutation	c.1396delA
AA Mutation	p.Ser466ValfsTer69(p.S466Vfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465261
Start	75807909:75807909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.930delT
AA Mutation	p.Glu312AsnfsTer33(p.E312Nfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000465261
Start	75817272:75817272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359G>A
AA Mutation	p.Trp453Ter(p.W453*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465261
Start	75849210:75849211(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3583_3584insA
AA Mutation	p.Leu1195HisfsTer4(p.L1195Hfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000465261
Start	75833050:75833050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000465261
Start	75834225:75834225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2366-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript