ClinVar Miner

List of variants in gene PALB2 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.11C>T (p.Pro4Leu) rs45619737 0.00010
NM_024675.4(PALB2):c.2474G>C (p.Arg825Thr) rs146218439 0.00008
NM_024675.4(PALB2):c.3428T>A (p.Leu1143His) rs62625284 0.00006
NM_024675.4(PALB2):c.1699C>T (p.His567Tyr) rs370422990 0.00004
NM_024675.4(PALB2):c.2106A>G (p.Ile702Met) rs730881886 0.00003
NM_024675.4(PALB2):c.2897T>C (p.Ile966Thr) rs587780214 0.00003
NM_024675.4(PALB2):c.2755G>A (p.Val919Ile) rs775193384 0.00002
NM_024675.4(PALB2):c.2978C>T (p.Thr993Met) rs61756146 0.00002
NM_024675.4(PALB2):c.749T>C (p.Leu250Ser) rs774675771 0.00001
NM_024675.4(PALB2):c.160_163delinsCAAG (p.Glu54_Gln55delinsGlnGlu) rs2142456599
NM_024675.4(PALB2):c.1748T>C (p.Leu583Ser) rs587782151
NM_024675.4(PALB2):c.2302T>C (p.Cys768Arg) rs1597089419
NM_024675.4(PALB2):c.2484C>G (p.Cys828Trp) rs875989798
NM_024675.4(PALB2):c.2561A>G (p.Asn854Ser) rs146455175
NM_024675.4(PALB2):c.2587-1G>C rs761214886
NM_024675.4(PALB2):c.2663T>C (p.Ile888Thr)
NM_024675.4(PALB2):c.3202-8G>A rs367979106
NM_024675.4(PALB2):c.3401C>G (p.Ser1134Cys)
NM_024675.4(PALB2):c.3496G>A (p.Gly1166Ser) rs1966397121
NM_024675.4(PALB2):c.623A>T (p.Asp208Val) rs1555461702

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