ClinVar Miner

List of variants in gene LAMB3 reported as uncertain significance by Invitae

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_000228.3(LAMB3):c.3404G>A (p.Arg1135Gln) rs115712132 0.00025
NM_000228.3(LAMB3):c.582G>T (p.Met194Ile) rs75876132 0.00019
NM_000228.3(LAMB3):c.911C>T (p.Pro304Leu) rs114394307 0.00019
NM_000228.3(LAMB3):c.1546A>G (p.Ile516Val) rs148988085 0.00012
NM_000228.3(LAMB3):c.1328C>T (p.Pro443Leu) rs202096620 0.00008
NM_000228.3(LAMB3):c.3434C>T (p.Ala1145Val) rs750121518 0.00006
NM_000228.3(LAMB3):c.2831A>G (p.Asn944Ser) rs567776263 0.00004
NM_000228.3(LAMB3):c.914C>T (p.Ala305Val) rs756331697 0.00004
NM_000228.3(LAMB3):c.707G>C (p.Ser236Thr) rs750934724 0.00003
NM_000228.3(LAMB3):c.1198G>C (p.Val400Leu) rs550298199 0.00002
NM_000228.3(LAMB3):c.10T>C (p.Phe4Leu)
NM_000228.3(LAMB3):c.116G>A (p.Arg39Gln)
NM_000228.3(LAMB3):c.1208A>G (p.Glu403Gly) rs2102425858
NM_000228.3(LAMB3):c.125G>A (p.Arg42Gln)
NM_000228.3(LAMB3):c.1639G>A (p.Asp547Asn)
NM_000228.3(LAMB3):c.1706G>A (p.Arg569Gln)
NM_000228.3(LAMB3):c.1886G>A (p.Ser629Asn)
NM_000228.3(LAMB3):c.2027T>C (p.Leu676Ser) rs1666321265
NM_000228.3(LAMB3):c.2237G>A (p.Arg746Gln)
NM_000228.3(LAMB3):c.2327C>T (p.Ser776Leu)
NM_000228.3(LAMB3):c.2518C>T (p.Arg840Trp)
NM_000228.3(LAMB3):c.2746G>A (p.Val916Met)
NM_000228.3(LAMB3):c.28+4A>C rs2102467676
NM_000228.3(LAMB3):c.2873G>A (p.Arg958His) rs142984572
NM_000228.3(LAMB3):c.2912G>A (p.Ser971Asn)
NM_000228.3(LAMB3):c.2962C>T (p.Arg988Trp) rs2229467
NM_000228.3(LAMB3):c.3125G>A (p.Arg1042Gln) rs749709873
NM_000228.3(LAMB3):c.3403C>T (p.Arg1135Trp)
NM_000228.3(LAMB3):c.3428G>A (p.Arg1143His)
NM_000228.3(LAMB3):c.388G>A (p.Gly130Ser)
NM_000228.3(LAMB3):c.514C>T (p.Arg172Trp)
NM_000228.3(LAMB3):c.828C>G (p.His276Gln)
NM_000228.3(LAMB3):c.898C>T (p.Arg300Trp)
NM_000228.3(LAMB3):c.943+3A>G
NM_000228.3(LAMB3):c.989C>T (p.Ala330Val)

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