List of variants reported as benign for melanoma, cutaneous malignant, susceptibility to, 8

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001354604.2(MITF):c.330G>A (p.Thr110=)	rs9849776	0.01713
NM_001354604.2(MITF):c.1566G>A (p.Thr522=)	rs36118030	0.00991
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.1031+14C>T	rs201353723	0.00077
NM_001354604.2(MITF):c.1182A>G (p.Glu394=)	rs137904015	0.00027
NM_001354604.2(MITF):c.1443G>A (p.Leu481=)	rs150213411	0.00027
NM_001354604.2(MITF):c.882G>A (p.Ala294=)	rs778126895	0.00011
NM_001354604.2(MITF):c.1381C>A (p.Leu461Ile)	rs78962087	0.00007
NM_001354604.2(MITF):c.1569G>A (p.Glu523=)	rs200830148	0.00003
NM_001354604.2(MITF):c.1517G>A (p.Gly506Glu)	rs548265796
NM_001354604.2(MITF):c.666+12C>T
NM_001354604.2(MITF):c.762+19dup

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