ClinVar Miner

List of variants in gene LAMC3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
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.1520-6G>A rs192031352 0.00175
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu) rs113443891 0.00123
NM_006059.4(LAMC3):c.558C>T (p.Arg186=) rs2275135 0.00105
NM_006059.4(LAMC3):c.2227A>G (p.Asn743Asp) rs36030184 0.00079
NM_006059.4(LAMC3):c.3674T>C (p.Val1225Ala) rs138481447 0.00068
NM_006059.4(LAMC3):c.2987G>A (p.Arg996His) rs113785045 0.00063
NM_006059.4(LAMC3):c.3489C>A (p.Ala1163=) rs200253736 0.00063
NM_006059.4(LAMC3):c.480C>T (p.Tyr160=) rs140728983 0.00044
NM_006059.4(LAMC3):c.4338G>A (p.Ala1446=) rs375730811 0.00041
NM_006059.4(LAMC3):c.3123C>T (p.Ser1041=) rs370140731 0.00036
NM_006059.4(LAMC3):c.4424G>A (p.Arg1475His) rs113354770 0.00033
NM_006059.4(LAMC3):c.2468A>G (p.Asn823Ser) rs140325029 0.00017
NM_006059.4(LAMC3):c.1051C>T (p.Arg351Cys) rs201626968 0.00014
NM_006059.4(LAMC3):c.696C>T (p.Thr232=) rs372132123 0.00009
NM_006059.4(LAMC3):c.2649G>A (p.Val883=) rs143175021 0.00008
NM_006059.4(LAMC3):c.2934C>T (p.His978=) rs1238180726 0.00006
NM_006059.4(LAMC3):c.3648G>A (p.Ala1216=) rs754510883 0.00005
NM_006059.4(LAMC3):c.3566C>T (p.Ala1189Val) rs369839636 0.00004
NM_006059.4(LAMC3):c.1130G>A (p.Arg377Gln) rs375139277 0.00002
NM_006059.4(LAMC3):c.2067G>A (p.Pro689=) rs149095454 0.00002
NM_006059.4(LAMC3):c.2924C>T (p.Ala975Val) rs756683242 0.00002
NM_006059.4(LAMC3):c.1414C>A (p.His472Asn) rs145387373 0.00001
NM_006059.4(LAMC3):c.2640C>T (p.Cys880=) rs770821754 0.00001
NM_006059.4(LAMC3):c.1557T>A (p.Ser519=)
NM_006059.4(LAMC3):c.2004C>G (p.Ser668=)
NM_006059.4(LAMC3):c.2307C>T (p.Ser769=)
NM_006059.4(LAMC3):c.2577C>T (p.Pro859=)
NM_006059.4(LAMC3):c.276C>T (p.Thr92=)
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>A (p.Arg1382=) rs147092908
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser) rs147092908

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