ClinVar Miner

List of variants in gene LIFR reported as uncertain significance for not provided

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Total variants: 19
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HGVS dbSNP
NM_001127671.2(LIFR):c.1171G>A (p.Glu391Lys)
NM_001127671.2(LIFR):c.1182ATT[2] (p.Leu396del) rs754991843
NM_001127671.2(LIFR):c.1357T>C (p.Trp453Arg) rs201516825
NM_001127671.2(LIFR):c.1460T>C (p.Val487Ala)
NM_001127671.2(LIFR):c.1485T>C (p.Ala495=) rs759537735
NM_001127671.2(LIFR):c.1516A>C (p.Thr506Pro) rs1057524477
NM_001127671.2(LIFR):c.1705C>G (p.Leu569Val)
NM_001127671.2(LIFR):c.2280G>A (p.Leu760=) rs370455274
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly) rs139848756
NM_001127671.2(LIFR):c.2336G>T (p.Gly779Val)
NM_001127671.2(LIFR):c.2591+6A>T
NM_001127671.2(LIFR):c.2887G>A (p.Ala963Thr)
NM_001127671.2(LIFR):c.2937G>A (p.Ser979=) rs201711670
NM_001127671.2(LIFR):c.2962GAA[2] (p.Glu990del)
NM_001127671.2(LIFR):c.3221A>G (p.Asp1074Gly) rs147058538
NM_001127671.2(LIFR):c.3275A>G (p.Gln1092Arg)
NM_001127671.2(LIFR):c.364A>G (p.Thr122Ala) rs145163157
NM_001127671.2(LIFR):c.452C>G (p.Ser151Cys) rs61751712
NM_001127671.2(LIFR):c.670A>G (p.Ile224Val) rs151282774

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