ClinVar Miner

List of variants in gene LAMA3 reported as benign by Invitae

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_198129.4(LAMA3):c.8500= (p.Gly2834=) rs1154233 0.99993
NM_198129.4(LAMA3):c.2901T>C (p.Ala967=) rs9962023 0.64176
NM_198129.4(LAMA3):c.9352-7G>A rs2241643 0.51794
NM_198129.4(LAMA3):c.4260G>C (p.Gly1420=) rs867449 0.48275
NM_198129.4(LAMA3):c.4530C>T (p.Pro1510=) rs12965685 0.47260
NM_198129.4(LAMA3):c.6147C>G (p.Ala2049=) rs1154226 0.21073
NM_198129.4(LAMA3):c.8445C>A (p.Asn2815Lys) rs1154232 0.17201
NM_198129.4(LAMA3):c.8731C>T (p.Leu2911=) rs1131521 0.15145
NM_198129.4(LAMA3):c.5322C>T (p.Phe1774=) rs958631 0.08419
NM_198129.4(LAMA3):c.4053C>T (p.Ala1351=) rs35035965 0.06429
NM_198129.4(LAMA3):c.3617T>C (p.Val1206Ala) rs12457323 0.05219
NM_198129.4(LAMA3):c.3622C>A (p.Pro1208Thr) rs17202961 0.05021
NM_198129.4(LAMA3):c.2387C>A (p.Thr796Asn) rs17187262 0.04907
NM_198129.4(LAMA3):c.3066C>G (p.Leu1022=) rs35756007 0.03848
NM_198129.4(LAMA3):c.6555C>T (p.Ala2185=) rs35872318 0.02513
NM_198129.4(LAMA3):c.57G>C (p.Thr19=) rs61752345 0.01596
NM_198129.4(LAMA3):c.8104A>G (p.Thr2702Ala) rs9952370 0.01207
NM_198129.4(LAMA3):c.4515T>C (p.Asp1505=) rs35565501 0.01146
NM_198129.4(LAMA3):c.433T>C (p.Leu145=) rs115800115 0.00779
NM_198129.4(LAMA3):c.9643-14C>T rs72875942 0.00748
NM_198129.4(LAMA3):c.1806G>A (p.Lys602=) rs34713637 0.00662
NM_198129.4(LAMA3):c.9353G>A (p.Ser3118Asn) rs61749943 0.00618
NM_198129.4(LAMA3):c.7797C>T (p.Asp2599=) rs61751706 0.00523
NM_198129.4(LAMA3):c.7818G>A (p.Thr2606=) rs139567388 0.00426
NM_198129.4(LAMA3):c.5012G>T (p.Gly1671Val) rs142097786 0.00351
NM_198129.4(LAMA3):c.4110G>A (p.Glu1370=) rs112534534 0.00336
NM_198129.4(LAMA3):c.9590A>G (p.His3197Arg) rs112073265 0.00333
NM_198129.4(LAMA3):c.3371T>G (p.Leu1124Arg) rs76711437 0.00312
NM_198129.4(LAMA3):c.6805C>G (p.Leu2269Val) rs138591939 0.00303
NM_198129.4(LAMA3):c.8629C>T (p.His2877Tyr) rs35153125 0.00264
NM_198129.4(LAMA3):c.8028C>T (p.Asn2676=) rs35737354 0.00238
NM_198129.4(LAMA3):c.4060G>A (p.Glu1354Lys) rs34799994 0.00224
NM_198129.4(LAMA3):c.891G>A (p.Gly297=) rs62093355 0.00223
NM_198129.4(LAMA3):c.9559C>T (p.Arg3187Cys) rs150956802 0.00200
NM_198129.4(LAMA3):c.8177+8G>A rs186430384 0.00169
NM_198129.4(LAMA3):c.1196G>C (p.Gly399Ala) rs76572574 0.00155
NM_198129.4(LAMA3):c.9027-11G>A rs117781425 0.00152
NM_198129.4(LAMA3):c.7218C>T (p.Asp2406=) rs62093184 0.00134
NM_198129.4(LAMA3):c.8898C>T (p.Ser2966=) rs141164795 0.00121
NM_198129.4(LAMA3):c.8829G>A (p.Arg2943=) rs141472847 0.00103
NM_198129.4(LAMA3):c.5223-13G>C rs145241852 0.00095
NM_198129.4(LAMA3):c.7905G>C (p.Leu2635=) rs138571165 0.00069
NM_198129.4(LAMA3):c.2769A>G (p.Ala923=) rs80345815 0.00044
NM_198129.4(LAMA3):c.4557C>T (p.Val1519=) rs202215313 0.00040
NM_198129.4(LAMA3):c.2996G>A (p.Arg999Gln) rs199976293 0.00034
NM_198129.4(LAMA3):c.5664A>C (p.Ile1888=) rs556283698 0.00031
NM_198129.4(LAMA3):c.7505A>G (p.Asn2502Ser) rs139823161 0.00029
NM_198129.4(LAMA3):c.2374G>A (p.Val792Ile) rs200330511 0.00026
NM_198129.4(LAMA3):c.8940C>T (p.Thr2980=) rs748453919 0.00025
NM_198129.4(LAMA3):c.9165G>A (p.Leu3055=) rs370470226 0.00018
NM_198129.4(LAMA3):c.4500C>T (p.Asn1500=) rs12607747 0.00017
NM_198129.4(LAMA3):c.5178C>T (p.Ala1726=) rs143755166 0.00011
NM_198129.4(LAMA3):c.3615A>G (p.Leu1205=) rs368047900 0.00010
NM_198129.4(LAMA3):c.3171T>C (p.Tyr1057=) rs142574930 0.00009
NM_198129.4(LAMA3):c.8500G>A (p.Gly2834Ser) rs1154233 0.00007
NM_198129.4(LAMA3):c.3002C>T (p.Ala1001Val) rs201043541 0.00005
NM_198129.4(LAMA3):c.312T>C (p.Tyr104=) rs376865778 0.00001
NM_198129.4(LAMA3):c.1901A>G (p.His634Arg)
NM_198129.4(LAMA3):c.2206G>A (p.Gly736Ser)
NM_198129.4(LAMA3):c.267C>T (p.Thr89=) rs534288868
NM_198129.4(LAMA3):c.3419C>T (p.Thr1140Met)
NM_198129.4(LAMA3):c.3932C>T (p.Pro1311Leu)
NM_198129.4(LAMA3):c.4545C>T (p.Ser1515=)
NM_198129.4(LAMA3):c.599G>A (p.Arg200Gln)
NM_198129.4(LAMA3):c.6202-12del
NM_198129.4(LAMA3):c.6202-13_6202-12del
NM_198129.4(LAMA3):c.6319-4del rs746830734
NM_198129.4(LAMA3):c.6319-4dup rs746830734
NM_198129.4(LAMA3):c.7016-12del
NM_198129.4(LAMA3):c.7016-12dup
NM_198129.4(LAMA3):c.7329+18A>G
NM_198129.4(LAMA3):c.79C>A (p.Arg27=)
NM_198129.4(LAMA3):c.8576+7G>C rs1258107
NM_198129.4(LAMA3):c.8576+7G>T rs1258107
NM_198129.4(LAMA3):c.8709-5del
NM_198129.4(LAMA3):c.9027-13A>G

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