ClinVar Miner

List of variants in gene NF1 reported as uncertain significance by Mendelics

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Total variants: 31
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HGVS dbSNP
NM_000267.3(NF1):c.1370A>T (p.His457Leu) rs786202763
NM_000267.3(NF1):c.1891G>A (p.Gly631Arg) rs757424379
NM_000267.3(NF1):c.2032C>A (p.Pro678Thr) rs758691069
NM_000267.3(NF1):c.2033C>T (p.Pro678Leu) rs17881753
NM_000267.3(NF1):c.2248A>G (p.Thr750Ala) rs748064845
NM_000267.3(NF1):c.2896G>A (p.Ala966Thr) rs876658849
NM_000267.3(NF1):c.2897C>G (p.Ala966Gly) rs1567849533
NM_000267.3(NF1):c.3436G>A (p.Val1146Ile) rs201047812
NM_000267.3(NF1):c.3625G>C (p.Val1209Leu) rs1458579232
NM_000267.3(NF1):c.3989A>C (p.Glu1330Ala) rs1256727206
NM_000267.3(NF1):c.4009C>T (p.Arg1337Trp) rs146306756
NM_000267.3(NF1):c.4199C>T (p.Pro1400Leu) rs753997885
NM_000267.3(NF1):c.4265C>T (p.Ser1422Leu) rs1555618566
NM_000267.3(NF1):c.4592A>G (p.Lys1531Arg) rs1172780277
NM_000267.3(NF1):c.4619G>A (p.Ser1540Asn) rs751414513
NM_000267.3(NF1):c.4771A>C (p.Arg1591=) rs755137259
NM_000267.3(NF1):c.484C>A (p.Gln162Lys) rs1555607073
NM_000267.3(NF1):c.4880C>T (p.Thr1627Ile) rs376655102
NM_000267.3(NF1):c.5843A>T (p.Gln1948Leu) rs143502927
NM_000267.3(NF1):c.6514G>C (p.Glu2172Gln)
NM_000267.3(NF1):c.6560C>T (p.Ala2187Val) rs1555534886
NM_000267.3(NF1):c.6574A>G (p.Met2192Val) rs864622330
NM_000267.3(NF1):c.6710G>A (p.Arg2237Gln) rs786202030
NM_000267.3(NF1):c.6943G>A (p.Ala2315Thr) rs587781428
NM_000267.3(NF1):c.7028G>A (p.Arg2343Gln) rs1555535407
NM_000267.3(NF1):c.7150A>G (p.Ile2384Val) rs565708398
NM_000267.3(NF1):c.7421C>T (p.Ser2474Phe) rs757245615
NM_000267.3(NF1):c.7450G>A (p.Ala2484Thr)
NM_000267.3(NF1):c.7637C>G (p.Pro2546Arg) rs754511534
NM_000267.3(NF1):c.8261A>G (p.Asn2754Ser) rs772090874
NM_000267.3(NF1):c.8332G>A (p.Val2778Ile) rs377393842

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