ClinVar Miner

List of variants in gene LAMA1 reported as uncertain significance by Ambry Genetics

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Total variants: 130
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HGVS dbSNP gnomAD frequency
NM_005559.4(LAMA1):c.1619C>T (p.Pro540Leu) rs140908403 0.00041
NM_005559.4(LAMA1):c.4211G>T (p.Ser1404Ile) rs147345095 0.00041
NM_005559.4(LAMA1):c.7187G>A (p.Arg2396Gln) rs200776408 0.00038
NM_005559.4(LAMA1):c.4612C>T (p.Arg1538Trp) rs149937004 0.00033
NM_005559.4(LAMA1):c.7600C>T (p.Arg2534Trp) rs376978539 0.00033
NM_005559.4(LAMA1):c.7847G>A (p.Arg2616Lys) rs144672024 0.00029
NM_005559.4(LAMA1):c.2323G>A (p.Gly775Ser) rs28369373 0.00028
NM_005559.4(LAMA1):c.1796C>T (p.Thr599Met) rs148234507 0.00026
NM_005559.4(LAMA1):c.6760G>A (p.Gly2254Arg) rs140199044 0.00017
NM_005559.4(LAMA1):c.4877C>T (p.Thr1626Met) rs201454996 0.00014
NM_005559.4(LAMA1):c.858+1G>T rs141914419 0.00012
NM_005559.4(LAMA1):c.2675A>G (p.Asp892Gly) rs374593442 0.00011
NM_005559.4(LAMA1):c.3503C>T (p.Thr1168Ile) rs779664777 0.00010
NM_005559.4(LAMA1):c.6012A>G (p.Ile2004Met) rs773225748 0.00007
NM_005559.4(LAMA1):c.3659G>A (p.Arg1220Gln) rs367987988 0.00006
NM_005559.4(LAMA1):c.2699G>A (p.Arg900His) rs945345901 0.00003
NM_005559.4(LAMA1):c.3152C>T (p.Ser1051Leu) rs758572977 0.00003
NM_005559.4(LAMA1):c.5840G>A (p.Arg1947His) rs569445597 0.00002
NM_005559.4(LAMA1):c.8314C>T (p.Arg2772Cys) rs760542877 0.00002
NM_005559.4(LAMA1):c.1197T>G (p.Cys399Trp) rs1568043232 0.00001
NM_005559.4(LAMA1):c.3181G>A (p.Gly1061Ser) rs768468360 0.00001
NM_005559.4(LAMA1):c.3580G>T (p.Val1194Phe) rs767031029 0.00001
NM_005559.4(LAMA1):c.3838G>A (p.Gly1280Arg) rs761791387 0.00001
NM_005559.4(LAMA1):c.4424G>A (p.Arg1475His) rs199872720 0.00001
NM_005559.4(LAMA1):c.8494G>T (p.Val2832Leu) rs1043223457 0.00001
NM_005559.4(LAMA1):c.101A>T (p.His34Leu)
NM_005559.4(LAMA1):c.1385C>A (p.Ala462Asp)
NM_005559.4(LAMA1):c.1393G>A (p.Glu465Lys)
NM_005559.4(LAMA1):c.1657A>G (p.Ser553Gly)
NM_005559.4(LAMA1):c.1721C>G (p.Ala574Gly)
NM_005559.4(LAMA1):c.1769C>T (p.Thr590Met) rs758586817
NM_005559.4(LAMA1):c.1961T>C (p.Ile654Thr)
NM_005559.4(LAMA1):c.206G>A (p.Cys69Tyr) rs1555664690
NM_005559.4(LAMA1):c.2153C>A (p.Thr718Asn)
NM_005559.4(LAMA1):c.220G>A (p.Ala74Thr)
NM_005559.4(LAMA1):c.221C>T (p.Ala74Val)
NM_005559.4(LAMA1):c.2245G>A (p.Ala749Thr)
NM_005559.4(LAMA1):c.2286C>A (p.His762Gln)
NM_005559.4(LAMA1):c.2465G>C (p.Gly822Ala)
NM_005559.4(LAMA1):c.2515C>T (p.Pro839Ser) rs143031283
NM_005559.4(LAMA1):c.2560A>C (p.Asn854His)
NM_005559.4(LAMA1):c.2578G>T (p.Ala860Ser)
NM_005559.4(LAMA1):c.2624G>A (p.Gly875Glu)
NM_005559.4(LAMA1):c.2630C>G (p.Thr877Arg)
NM_005559.4(LAMA1):c.2677G>A (p.Ala893Thr)
NM_005559.4(LAMA1):c.2746C>A (p.Leu916Ile)
NM_005559.4(LAMA1):c.2767T>C (p.Cys923Arg)
NM_005559.4(LAMA1):c.2771A>G (p.Lys924Arg)
NM_005559.4(LAMA1):c.2783C>T (p.Thr928Ile)
NM_005559.4(LAMA1):c.2869G>A (p.Gly957Ser)
NM_005559.4(LAMA1):c.2882A>G (p.Asp961Gly)
NM_005559.4(LAMA1):c.2891C>T (p.Thr964Met)
NM_005559.4(LAMA1):c.2966C>T (p.Ala989Val)
NM_005559.4(LAMA1):c.3063G>C (p.Gln1021His)
NM_005559.4(LAMA1):c.3127G>T (p.Ala1043Ser)
NM_005559.4(LAMA1):c.3363G>T (p.Lys1121Asn)
NM_005559.4(LAMA1):c.3507A>C (p.Pro1169=)
NM_005559.4(LAMA1):c.3617C>G (p.Ala1206Gly)
NM_005559.4(LAMA1):c.3625C>T (p.Arg1209Trp)
NM_005559.4(LAMA1):c.3626G>T (p.Arg1209Leu)
NM_005559.4(LAMA1):c.3665C>T (p.Pro1222Leu)
NM_005559.4(LAMA1):c.3748G>A (p.Gly1250Ser)
NM_005559.4(LAMA1):c.3958A>G (p.Ile1320Val)
NM_005559.4(LAMA1):c.4087G>A (p.Val1363Ile)
NM_005559.4(LAMA1):c.4142A>T (p.His1381Leu)
NM_005559.4(LAMA1):c.416G>A (p.Arg139His)
NM_005559.4(LAMA1):c.4241C>T (p.Pro1414Leu)
NM_005559.4(LAMA1):c.4285G>C (p.Asp1429His)
NM_005559.4(LAMA1):c.4494C>A (p.Asn1498Lys)
NM_005559.4(LAMA1):c.4543G>A (p.Gly1515Ser)
NM_005559.4(LAMA1):c.4588T>C (p.Cys1530Arg)
NM_005559.4(LAMA1):c.4715G>C (p.Gly1572Ala)
NM_005559.4(LAMA1):c.4741A>G (p.Thr1581Ala)
NM_005559.4(LAMA1):c.4966G>T (p.Asp1656Tyr)
NM_005559.4(LAMA1):c.5014A>G (p.Met1672Val)
NM_005559.4(LAMA1):c.5082_5093del (p.Met1695_Asn1698del)
NM_005559.4(LAMA1):c.5257G>A (p.Val1753Ile)
NM_005559.4(LAMA1):c.5450T>C (p.Ile1817Thr)
NM_005559.4(LAMA1):c.5454T>G (p.Asp1818Glu)
NM_005559.4(LAMA1):c.5497C>T (p.His1833Tyr)
NM_005559.4(LAMA1):c.5726T>C (p.Ile1909Thr) rs199766289
NM_005559.4(LAMA1):c.5870A>T (p.Asn1957Ile)
NM_005559.4(LAMA1):c.5935T>A (p.Phe1979Ile)
NM_005559.4(LAMA1):c.6067G>A (p.Val2023Met)
NM_005559.4(LAMA1):c.6131C>T (p.Ser2044Phe) rs142732096
NM_005559.4(LAMA1):c.6203G>T (p.Gly2068Val)
NM_005559.4(LAMA1):c.6325G>T (p.Ala2109Ser)
NM_005559.4(LAMA1):c.6341C>G (p.Ala2114Gly)
NM_005559.4(LAMA1):c.6355G>A (p.Ala2119Thr)
NM_005559.4(LAMA1):c.6410C>T (p.Thr2137Ile)
NM_005559.4(LAMA1):c.6413A>G (p.Asn2138Ser)
NM_005559.4(LAMA1):c.6442A>T (p.Thr2148Ser)
NM_005559.4(LAMA1):c.6505G>A (p.Val2169Met)
NM_005559.4(LAMA1):c.6515G>A (p.Arg2172Gln)
NM_005559.4(LAMA1):c.6524G>C (p.Arg2175Thr)
NM_005559.4(LAMA1):c.6551C>T (p.Ser2184Phe)
NM_005559.4(LAMA1):c.6563G>A (p.Arg2188His)
NM_005559.4(LAMA1):c.6577G>T (p.Asp2193Tyr)
NM_005559.4(LAMA1):c.6715G>A (p.Val2239Ile)
NM_005559.4(LAMA1):c.6770T>G (p.Ile2257Ser)
NM_005559.4(LAMA1):c.679C>T (p.Arg227Cys)
NM_005559.4(LAMA1):c.6877A>G (p.Lys2293Glu)
NM_005559.4(LAMA1):c.6934G>A (p.Gly2312Arg)
NM_005559.4(LAMA1):c.6976G>A (p.Val2326Met)
NM_005559.4(LAMA1):c.7037G>T (p.Gly2346Val)
NM_005559.4(LAMA1):c.7078C>T (p.Arg2360Cys)
NM_005559.4(LAMA1):c.7090A>G (p.Lys2364Glu)
NM_005559.4(LAMA1):c.7092G>C (p.Lys2364Asn)
NM_005559.4(LAMA1):c.7253A>G (p.Glu2418Gly)
NM_005559.4(LAMA1):c.7309G>A (p.Gly2437Ser)
NM_005559.4(LAMA1):c.730C>T (p.Arg244Trp)
NM_005559.4(LAMA1):c.7490T>A (p.Ile2497Asn)
NM_005559.4(LAMA1):c.754A>G (p.Ile252Val)
NM_005559.4(LAMA1):c.7589A>T (p.Asp2530Val)
NM_005559.4(LAMA1):c.7922G>A (p.Arg2641Lys)
NM_005559.4(LAMA1):c.7945A>C (p.Asn2649His)
NM_005559.4(LAMA1):c.8308G>C (p.Gly2770Arg)
NM_005559.4(LAMA1):c.8375T>A (p.Leu2792His)
NM_005559.4(LAMA1):c.8443G>A (p.Gly2815Ser)
NM_005559.4(LAMA1):c.8455C>G (p.Pro2819Ala)
NM_005559.4(LAMA1):c.8555A>C (p.Asn2852Thr)
NM_005559.4(LAMA1):c.8566A>C (p.Ser2856Arg)
NM_005559.4(LAMA1):c.8649C>G (p.Asn2883Lys)
NM_005559.4(LAMA1):c.8689G>A (p.Gly2897Arg)
NM_005559.4(LAMA1):c.8695G>A (p.Gly2899Arg)
NM_005559.4(LAMA1):c.873A>T (p.Gln291His)
NM_005559.4(LAMA1):c.8775G>C (p.Gln2925His)
NM_005559.4(LAMA1):c.8839G>C (p.Gly2947Arg)
NM_005559.4(LAMA1):c.892G>C (p.Gly298Arg) rs565276715
NM_005559.4(LAMA1):c.8996G>A (p.Gly2999Asp)

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