ClinVar Miner

List of variants in gene WDR62 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_001083961.2(WDR62):c.10G>C (p.Val4Leu) rs147077663
NM_001083961.2(WDR62):c.1129G>T (p.Val377Leu) rs761204875
NM_001083961.2(WDR62):c.1233+7C>G rs537771936
NM_001083961.2(WDR62):c.1640C>T (p.Thr547Met) rs756313871
NM_001083961.2(WDR62):c.2269C>G (p.Leu757Val) rs150593960
NM_001083961.2(WDR62):c.2560G>A (p.Ala854Thr) rs368030329
NM_001083961.2(WDR62):c.2674G>A (p.Glu892Lys) rs1349805169
NM_001083961.2(WDR62):c.3309C>A (p.Phe1103Leu) rs1064797238
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) rs146180208
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) rs147652186
NM_001083961.2(WDR62):c.4312-5T>G rs182467995
NM_001083961.2(WDR62):c.4329G>A (p.Gln1443=) rs771131709
NM_001083961.2(WDR62):c.553G>A (p.Asp185Asn) rs1393055537
NM_001083961.2(WDR62):c.700G>T (p.Val234Leu) rs1216375665
NM_001083961.2(WDR62):c.761_763TCT[1] (p.Phe255del) rs1064797236

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