ClinVar Miner

List of variants in gene LAMC3 reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_006059.4(LAMC3):c.219T>G (p.His73Gln) rs3739512 0.56936
NM_006059.4(LAMC3):c.1564C>T (p.Pro522Ser) rs869457 0.28273
NM_006059.4(LAMC3):c.75C>T (p.Cys25=) rs13286358 0.10217
NM_006059.4(LAMC3):c.92G>T (p.Arg31Leu) rs116259120 0.02047
NM_006059.4(LAMC3):c.-2C>T rs137883250 0.01424
NM_006059.4(LAMC3):c.146A>G (p.Gln49Arg) rs201962705 0.00645
NM_006059.4(LAMC3):c.4092C>T (p.Ser1364=) rs141724499 0.00360
NM_006059.4(LAMC3):c.2891-8C>T rs199535979 0.00339
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=) rs140540789 0.00292
NM_006059.4(LAMC3):c.4160C>T (p.Ala1387Val) rs141497885 0.00258
NM_006059.4(LAMC3):c.3927+8C>G rs148008251 0.00228
NM_006059.4(LAMC3):c.3347C>G (p.Ala1116Gly) rs36028197 0.00226
NM_006059.4(LAMC3):c.1630+5C>G rs184221540 0.00178
NM_006059.4(LAMC3):c.1520-6G>A rs192031352 0.00175
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu) rs113443891 0.00123
NM_006059.4(LAMC3):c.3409G>C (p.Ala1137Pro) rs149766298 0.00041
NM_006059.4(LAMC3):c.1019G>A (p.Arg340Gln) rs149004188 0.00037
NM_006059.4(LAMC3):c.4068G>A (p.Ala1356=) rs377618961 0.00008
NM_006059.4(LAMC3):c.3607A>T (p.Thr1203Ser) rs141639990 0.00006
NM_006059.4(LAMC3):c.2430C>A (p.Cys810Ter) rs769118642 0.00002
NM_006059.4(LAMC3):c.3624G>A (p.Glu1208=) rs569440839 0.00002
NM_006059.4(LAMC3):c.4031-10G>A rs555619019 0.00001
NM_006059.4(LAMC3):c.4698C>T (p.Ser1566=) rs754122699 0.00001
NM_006059.4(LAMC3):c.4705G>A (p.Glu1569Lys) rs145287578 0.00001
NM_006059.4(LAMC3):c.1939G>C (p.Gly647Arg) rs144242690
NM_006059.4(LAMC3):c.2438_2439delinsAG (p.Ser813Lys) rs386738959
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln) rs146221263
NM_006059.4(LAMC3):c.3379G>A (p.Glu1127Lys) rs140955110
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser) rs147092908
NM_006059.4(LAMC3):c.422G>A (p.Arg141His) rs756873191
NM_006059.4(LAMC3):c.521_522delinsAG (p.Pro174Gln) rs386738954

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