ClinVar Miner

List of variants in gene NEXMIF reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_001008537.3(NEXMIF):c.3555G>T (p.Gly1185=) rs142714242 0.00059
NM_001008537.3(NEXMIF):c.2139G>A (p.Glu713=) rs139194076 0.00055
NM_001008537.3(NEXMIF):c.2505C>T (p.His835=) rs143453497 0.00038
NM_001008537.3(NEXMIF):c.4320C>T (p.Asn1440=) rs769979162 0.00027
NM_001008537.3(NEXMIF):c.347A>G (p.Asn116Ser) rs147908044 0.00026
NM_001008537.3(NEXMIF):c.3775G>A (p.Ala1259Thr) rs761368099 0.00022
NM_001008537.3(NEXMIF):c.4048G>A (p.Asp1350Asn) rs200982385 0.00017
NM_001008537.3(NEXMIF):c.313A>C (p.Ile105Leu) rs141738108 0.00014
NM_001008537.3(NEXMIF):c.1854G>A (p.Glu618=) rs142687313 0.00012
NM_001008537.3(NEXMIF):c.357G>A (p.Glu119=) rs142318614 0.00012
NM_001008537.3(NEXMIF):c.3753A>G (p.Ile1251Met) rs143365662 0.00012
NM_001008537.3(NEXMIF):c.3823A>G (p.Ser1275Gly) rs201434271 0.00012
NM_001008537.3(NEXMIF):c.1712G>A (p.Ser571Asn) rs372044888 0.00010
NM_001008537.3(NEXMIF):c.1983C>T (p.His661=) rs138583612 0.00010
NM_001008537.3(NEXMIF):c.2851G>A (p.Asp951Asn) rs771918287 0.00010
NM_001008537.3(NEXMIF):c.3001G>C (p.Val1001Leu) rs755462704 0.00010
NM_001008537.3(NEXMIF):c.3812T>C (p.Met1271Thr) rs138236888 0.00010
NM_001008537.3(NEXMIF):c.4446T>G (p.Phe1482Leu) rs770781682 0.00008
NM_001008537.3(NEXMIF):c.4043A>G (p.His1348Arg) rs779047497 0.00007
NM_001008537.3(NEXMIF):c.4368C>A (p.Ala1456=) rs781623230 0.00006
NM_001008537.3(NEXMIF):c.3479A>G (p.Asn1160Ser) rs764370545 0.00005
NM_001008537.3(NEXMIF):c.1261C>T (p.Leu421Phe) rs1320278331 0.00004
NM_001008537.3(NEXMIF):c.2130G>A (p.Lys710=) rs749479992 0.00004
NM_001008537.3(NEXMIF):c.2784C>G (p.Leu928=) rs754561437 0.00004
NM_001008537.3(NEXMIF):c.2966G>A (p.Arg989Gln) rs140836456 0.00004
NM_001008537.3(NEXMIF):c.4217C>A (p.Ala1406Glu) rs775633155 0.00004
NM_001008537.3(NEXMIF):c.783C>T (p.Phe261=) rs768534908 0.00004
NM_001008537.3(NEXMIF):c.153G>A (p.Pro51=) rs147096194 0.00003
NM_001008537.3(NEXMIF):c.2544C>T (p.Thr848=) rs139924662 0.00003
NM_001008537.3(NEXMIF):c.2786C>T (p.Thr929Ile) rs370164571 0.00002
NM_001008537.3(NEXMIF):c.1196A>G (p.Asp399Gly) rs776363168 0.00001
NM_001008537.3(NEXMIF):c.1877G>A (p.Arg626His) rs201084618 0.00001
NM_001008537.3(NEXMIF):c.2331T>C (p.His777=) rs762407174 0.00001
NM_001008537.3(NEXMIF):c.3294C>T (p.Phe1098=) rs756252858 0.00001
NM_001008537.3(NEXMIF):c.3323G>A (p.Ser1108Asn) rs763992609 0.00001
NM_001008537.3(NEXMIF):c.653G>A (p.Arg218Gln) rs747496798 0.00001
NM_001008537.3(NEXMIF):c.154G>A (p.Val52Met) rs747414246
NM_001008537.3(NEXMIF):c.1683G>A (p.Val561=)
NM_001008537.3(NEXMIF):c.1741C>T (p.Leu581=) rs1569335620
NM_001008537.3(NEXMIF):c.1749C>G (p.Pro583=) rs776062521
NM_001008537.3(NEXMIF):c.1768AAG[3] (p.Lys593del) rs752119872
NM_001008537.3(NEXMIF):c.2150T>C (p.Leu717Pro)
NM_001008537.3(NEXMIF):c.2796A>G (p.Thr932=)
NM_001008537.3(NEXMIF):c.306A>G (p.Thr102=)
NM_001008537.3(NEXMIF):c.3325G>A (p.Val1109Met) rs948687949
NM_001008537.3(NEXMIF):c.3439G>C (p.Val1147Leu) rs1569335080
NM_001008537.3(NEXMIF):c.3444C>T (p.Ser1148=)
NM_001008537.3(NEXMIF):c.3776C>A (p.Ala1259Asp)
NM_001008537.3(NEXMIF):c.4177A>C (p.Arg1393=)
NM_001008537.3(NEXMIF):c.4493C>A (p.Thr1498Asn)

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