Mutation

Primary Site >> Stomach Cancer

Gene >> LRBA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150852140:150852140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3570G>A
AA Mutation	p.Met1190Ile(p.M1190I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150302708:150302708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775871299
CDS Mutation	c.7967A>T
AA Mutation	p.Tyr2656Phe(p.Y2656F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150844755:150844755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772088099
CDS Mutation	c.4364G>A
AA Mutation	p.Cys1455Tyr(p.C1455Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357115
Start	150471737:150471737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760622773
CDS Mutation	c.6587G>A
AA Mutation	p.Arg2196His(p.R2196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150897779:150897779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542115160
CDS Mutation	c.1964G>A
AA Mutation	p.Arg655Gln(p.R655Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150915625:150915625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997T>G
AA Mutation	p.Phe333Val(p.F333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150467758:150467758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6728A>G
AA Mutation	p.Tyr2243Cys(p.Y2243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150849468:150849468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4112C>A
AA Mutation	p.Ala1371Asp(p.A1371D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150828517:150828517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4834G>A
AA Mutation	p.Ala1612Thr(p.A1612T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150277881:150277881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143351602
CDS Mutation	c.8473C>T
AA Mutation	p.Arg2825Trp(p.R2825W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150435609:150435609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139428686
CDS Mutation	c.7054C>T
AA Mutation	p.Arg2352Cys(p.R2352C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150906319:150906319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580T>C
AA Mutation	p.Val527Ala(p.V527A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150928520:150928520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769037604
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150905944:150905944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781408716
CDS Mutation	c.1649C>T
AA Mutation	p.Ala550Val(p.A550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150828453:150828453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4898G>A
AA Mutation	p.Gly1633Asp(p.G1633D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150817243:150817243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5186C>G
AA Mutation	p.Ala1729Gly(p.A1729G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150321299:150321299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7555C>G
AA Mutation	p.Pro2519Ala(p.P2519A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150302732:150302732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7943A>T
AA Mutation	p.Glu2648Val(p.E2648V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150487757:150487757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756885055
CDS Mutation	c.6559A>G
AA Mutation	p.Thr2187Ala(p.T2187A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150928559:150928559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>A
AA Mutation	p.Leu169Gln(p.L169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150852028:150852028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3682T>C
AA Mutation	p.Cys1228Arg(p.C1228R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150599057:150599057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5996C>G
AA Mutation	p.Pro1999Arg(p.P1999R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150415484:150415484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7181C>T
AA Mutation	p.Pro2394Leu(p.P2394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000357115
Start	150908826:150908826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1193T>C
AA Mutation	p.Leu398Pro(p.L398P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150915652:150915652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150735297:150735297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5715G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150277861:150277861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76608264
CDS Mutation	c.8493C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150828587:150828587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144797074
CDS Mutation	c.4764G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150893093:150893093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150277870:150277870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566917747
CDS Mutation	c.8484G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150852482:150852482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3228T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150467739:150467739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6747C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150599032:150599032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138018109
CDS Mutation	c.6021G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150590765:150590765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6174C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150315607:150315607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201178305
CDS Mutation	c.7680A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357115
Start	150683667:150683667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5805T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357115
Start	150852902:150852902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2808delT
AA Mutation	p.Phe936LeufsTer12(p.F936Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357115
Start	150599022:150599022(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6031delA
AA Mutation	p.Thr2011GlnfsTer11(p.T2011Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357115
Start	150588058:150588059(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6352dupA
AA Mutation	p.Ile2118AsnfsTer61(p.I2118Nfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	40
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357115
Start	150590712:150590712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6226+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	41
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357115
Start	150896457:150896457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2005-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript