ClinVar Miner

List of variants in gene LOC105369149, SBF2 studied for Charcot-Marie-Tooth disease type 4B2

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_030962.4(SBF2):c.4571-6C>T rs2645029 0.88084
NM_030962.4(SBF2):c.4933-15T>C rs75447733 0.03044
NM_030962.4(SBF2):c.5014_5016del (p.Lys1672del) rs750958357 0.00065
NM_030962.4(SBF2):c.4805A>G (p.Lys1602Arg) rs147772705 0.00048
NM_030962.4(SBF2):c.5037C>T (p.Arg1679=) rs200784979 0.00048
NM_030962.4(SBF2):c.5054C>G (p.Ser1685Trp) rs148468522 0.00048
NM_030962.4(SBF2):c.5058A>T (p.Arg1686Ser) rs146230559 0.00046
NM_030962.4(SBF2):c.4712A>G (p.Asn1571Ser) rs371960255 0.00011
NM_030962.4(SBF2):c.5037+12A>G rs372500490 0.00009
NM_030962.4(SBF2):c.5231+14C>T rs371184526 0.00008
NM_030962.4(SBF2):c.4932T>C (p.Ser1644=) rs757095964 0.00002
NM_030962.4(SBF2):c.5036G>A (p.Arg1679His) rs769919130 0.00002
NM_030962.4(SBF2):c.5231+13A>G rs1242027664 0.00002
NM_030962.4(SBF2):c.4733A>G (p.Lys1578Arg) rs775360425 0.00001
NM_030962.4(SBF2):c.4931G>A (p.Ser1644Asn) rs754078134 0.00001
NM_030962.4(SBF2):c.5035C>T (p.Arg1679Cys) rs79401259 0.00001
NM_030962.4(SBF2):c.5041C>T (p.Gln1681Ter) rs1343702415 0.00001
NM_030962.4(SBF2):c.5232-7C>A rs752774091 0.00001
NM_030962.4(SBF2):c.5365A>G (p.Ile1789Val) rs746542104 0.00001
NM_030962.4(SBF2):c.4825T>G (p.Ser1609Ala) rs1852579303
NM_030962.4(SBF2):c.4877del (p.Pro1626fs) rs1852575488
NM_030962.4(SBF2):c.5004C>G (p.Thr1668=) rs150598413
NM_030962.4(SBF2):c.5004C>T (p.Thr1668=) rs150598413
NM_030962.4(SBF2):c.5017GAA[1] (p.Glu1674del) rs572571832
NM_030962.4(SBF2):c.5135G>A (p.Gly1712Glu) rs757214892
NM_030962.4(SBF2):c.5179C>G (p.Arg1727Gly) rs750756174
NM_030962.4(SBF2):c.5198A>G (p.Tyr1733Cys) rs1334739235
NM_030962.4(SBF2):c.5203C>T (p.Gln1735Ter) rs1590076969
NM_030962.4(SBF2):c.5290del (p.Trp1764fs)
NM_030962.4(SBF2):c.5296G>A (p.Val1766Ile) rs886048779

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