Mutation

Primary Site >> Stomach Cancer

Gene >> LAMA3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23950112:23950112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775368078
CDS Mutation	c.9595G>A
AA Mutation	p.Gly3199Arg(p.G3199R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23946210:23946210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9277A>C
AA Mutation	p.Ser3093Arg(p.S3093R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23842416:23842416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778909276
CDS Mutation	c.3358C>T
AA Mutation	p.Arg1120Cys(p.R1120C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23861770:23861770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759552468
CDS Mutation	c.4547C>T
AA Mutation	p.Ala1516Val(p.A1516V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23846457:23846457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758622204
CDS Mutation	c.3880C>T
AA Mutation	p.Arg1294Trp(p.R1294W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23881962:23881962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5139G>T
AA Mutation	p.Glu1713Asp(p.E1713D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23894957:23894957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533403846
CDS Mutation	c.5512G>A
AA Mutation	p.Glu1838Lys(p.E1838K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23748016:23748016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521C>T
AA Mutation	p.Ser174Phe(p.S174F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23903113:23903113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6306G>T
AA Mutation	p.Glu2102Asp(p.E2102D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23904050:23904050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146005577
CDS Mutation	c.6436G>A
AA Mutation	p.Ala2146Thr(p.A2146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23904663:23904663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6584G>T
AA Mutation	p.Arg2195Met(p.R2195M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23914546:23914546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745326570
CDS Mutation	c.7466G>A
AA Mutation	p.Arg2489Gln(p.R2489Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23931122:23931122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8497G>T
AA Mutation	p.Gly2833Cys(p.G2833C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23946244:23946244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571009750
CDS Mutation	c.9311C>T
AA Mutation	p.Ala3104Val(p.A3104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23916622:23916622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7850C>T
AA Mutation	p.Ala2617Val(p.A2617V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23928165:23928165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8220T>A
AA Mutation	p.Asn2740Lys(p.N2740K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23842485:23842485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750682821
CDS Mutation	c.3427G>A
AA Mutation	p.Ala1143Thr(p.A1143T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23921014:23921014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8003G>C
AA Mutation	p.Arg2668Thr(p.R2668T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23899385:23899385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5934G>T
AA Mutation	p.Arg1978Ser(p.R1978S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23819924:23819924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2231T>C
AA Mutation	p.Leu744Pro(p.L744P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23921482:23921482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768962336
CDS Mutation	c.8074C>T
AA Mutation	p.Arg2692Cys(p.R2692C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23819861:23819861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2168T>A
AA Mutation	p.Phe723Tyr(p.F723Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23763473:23763473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132T>G
AA Mutation	p.Leu378Val(p.L378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23842516:23842516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549221489
CDS Mutation	c.3458G>A
AA Mutation	p.Arg1153Gln(p.R1153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313654
Start	23819996:23819996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2303A>G
AA Mutation	p.Gln768Arg(p.Q768R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23751066:23751066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750852201
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23775816:23775816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777385606
CDS Mutation	c.1298C>T
AA Mutation	p.Ala433Val(p.A433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23914763:23914763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7547G>A
AA Mutation	p.Gly2516Glu(p.G2516E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000313654
Start	23951735:23951735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9694C>G
AA Mutation	p.Pro3232Ala(p.P3232A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23915318:23915318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7674C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23816455:23816455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23882007:23882007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144191865
CDS Mutation	c.5184C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23921526:23921526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8118T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23884821:23884821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774968902
CDS Mutation	c.5271C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23907859:23907859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6939G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23822341:23822341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2394A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23784126:23784126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23810499:23810499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313654
Start	23827458:23827458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188353268
CDS Mutation	c.2814C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313654
Start	23915376:23915376(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7738delA
AA Mutation	p.Thr2580HisfsTer68(p.T2580Hfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000313654
Start	23928208:23928208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8263G>T
AA Mutation	p.Gly2755Ter(p.G2755*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	stop_gained
Transcription ID	ENST00000313654
Start	23824513:23824513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2519C>A
AA Mutation	p.Ser840Ter(p.S840*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313654
Start	23758426:23758427(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.982dupG
AA Mutation	p.Glu328GlyfsTer4(p.E328Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	44
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000313654
Start	23777620:23777620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript