Mutation

Primary Site >> Stomach Cancer

Gene >> LRP5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68433754:68433754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748395267
CDS Mutation	c.3916G>A
AA Mutation	p.Ala1306Thr(p.A1306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68413949:68413949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773895575
CDS Mutation	c.2764G>A
AA Mutation	p.Gly922Ser(p.G922S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68433673:68433673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3835C>T
AA Mutation	p.Arg1279Cys(p.R1279C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68436987:68436987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28939709
CDS Mutation	c.4099G>A
AA Mutation	p.Glu1367Lys(p.E1367K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68413844:68413844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2659G>A
AA Mutation	p.Asp887Asn(p.D887N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68410067:68410067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2245G>A
AA Mutation	p.Gly749Arg(p.G749R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68448952:68448952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4730C>A
AA Mutation	p.Pro1577His(p.P1577H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68425131:68425131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373906355
CDS Mutation	c.3266G>A
AA Mutation	p.Arg1089Gln(p.R1089Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68363773:68363773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375404890
CDS Mutation	c.713C>T
AA Mutation	p.Thr238Met(p.T238M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68357822:68357822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765147716
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294304
Start	68357846:68357846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766589610
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68438484:68438484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4150A>C
AA Mutation	p.Ser1384Arg(p.S1384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68347927:68347927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>A
AA Mutation	p.Val58Met(p.V58M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294304
Start	68348242:68348242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748168729
CDS Mutation	c.487G>A
AA Mutation	p.Gly163Arg(p.G163R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68426059:68426059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3509T>A
AA Mutation	p.Ile1170Asn(p.I1170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68386442:68386442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142A>G
AA Mutation	p.Asp381Gly(p.D381G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68423588:68423588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3127G>A
AA Mutation	p.Glu1043Lys(p.E1043K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68413881:68413881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2696G>A
AA Mutation	p.Arg899His(p.R899H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68348111:68348111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Asp(p.G119D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68409956:68409956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765239493
CDS Mutation	c.2134G>A
AA Mutation	p.Val712Met(p.V712M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68425256:68425256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3391G>A
AA Mutation	p.Ala1131Thr(p.A1131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68429593:68429593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143924910
CDS Mutation	c.3656G>A
AA Mutation	p.Arg1219His(p.R1219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68386568:68386568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268T>C
AA Mutation	p.Val423Ala(p.V423A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68416382:68416382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189095829
CDS Mutation	c.2882C>T
AA Mutation	p.Pro961Leu(p.P961L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68433778:68433778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373750800
CDS Mutation	c.3940C>T
AA Mutation	p.Arg1314Cys(p.R1314C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68425109:68425109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3244T>C
AA Mutation	p.Tyr1082His(p.Y1082H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68448844:68448844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150862227
CDS Mutation	c.4622C>T
AA Mutation	p.Thr1541Met(p.T1541M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68433799:68433799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3961G>A
AA Mutation	p.Ala1321Thr(p.A1321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000294304
Start	68426085:68426085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780585577
CDS Mutation	c.3535C>T
AA Mutation	p.Arg1179Cys(p.R1179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68386500:68386500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774484799
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68386422:68386422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764504521
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68357680:68357680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148128016
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68448845:68448845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139974816
CDS Mutation	c.4623G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68347983:68347983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294304
Start	68433696:68433696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768877066
CDS Mutation	c.3858C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294304
Start	68365625:68365625(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.941delC
AA Mutation	p.Pro314GlnfsTer70(p.P314Qfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294304
Start	68348111:68348117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.358_364delAAGAAGC
AA Mutation	p.Lys120CysfsTer79(p.K120Cfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000294304
Start	68416504:68416504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3004C>T
AA Mutation	p.Arg1002Ter(p.R1002*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000294304
Start	68425294:68425294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3427+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript