ClinVar Miner

List of variants in gene MITF reported as likely benign for not specified

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001354604.2(MITF):c.880+9C>G rs181810413 0.00203
NM_001354604.2(MITF):c.366C>T (p.His122=) rs140663277 0.00201
NM_001354604.2(MITF):c.1280T>C (p.Val427Ala) rs2055006 0.00094
NM_001354604.2(MITF):c.1182A>G (p.Glu394=) rs137904015 0.00027
NM_001354604.2(MITF):c.114C>T (p.Ala38=) rs374097282 0.00021
NM_001354604.2(MITF):c.667-3C>T rs376704147 0.00021
NM_001354604.2(MITF):c.955+40A>T rs780050293 0.00020
NM_001354604.2(MITF):c.666+15G>C rs201698367 0.00012
NM_001354604.2(MITF):c.537C>T (p.Asn179=) rs150591206 0.00008
NM_001354604.2(MITF):c.345A>G (p.Glu115=) rs370482858 0.00006
NM_001354604.2(MITF):c.623A>G (p.Glu208Gly) rs200108255 0.00006
NM_001354604.2(MITF):c.667-7C>T rs201271211 0.00006
NM_001354604.2(MITF):c.1494A>C (p.Pro498=) rs777982903 0.00004
NM_001354604.2(MITF):c.1031+15G>A rs144757214 0.00003
NM_001354604.2(MITF):c.105-12836C>T rs779387274 0.00003
NM_001354604.2(MITF):c.1179+4C>T rs749869303 0.00003
NM_001354604.2(MITF):c.513G>A (p.Pro171=) rs774998383 0.00003
NM_001354604.2(MITF):c.1476C>T (p.Pro492=) rs745749254 0.00001
NM_001354604.2(MITF):c.666+8A>G rs560348035 0.00001
NM_001354604.2(MITF):c.763-50C>A rs756211227 0.00001
NM_001354604.2(MITF):c.105-40T>C rs1226144443
NM_001354604.2(MITF):c.1050G>A (p.Lys350=) rs201348324
NM_001354604.2(MITF):c.1150G>A (p.Ala384Thr) rs202020443
NM_001354604.2(MITF):c.1179+5G>A rs554738793
NM_001354604.2(MITF):c.956-7C>A rs886038272

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