ClinVar Miner

List of variants in gene HPS6 reported as uncertain significance for Hermansky-Pudlak syndrome without pulmonary fibrosis

Included ClinVar conditions (3):
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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_024747.5(HPS6):c.1039G>A (p.Val347Ile) rs139517839
NM_024747.5(HPS6):c.1060C>T (p.His354Tyr) rs149692177
NM_024747.5(HPS6):c.112C>G (p.Pro38Ala) rs746813506
NM_024747.5(HPS6):c.1181T>C (p.Val394Ala) rs146521433
NM_024747.5(HPS6):c.1201G>A (p.Asp401Asn) rs886046651
NM_024747.5(HPS6):c.138G>A (p.Leu46=) rs886046648
NM_024747.5(HPS6):c.1606A>G (p.Arg536Gly) rs757589760
NM_024747.5(HPS6):c.194C>G (p.Ala65Gly) rs886046649
NM_024747.5(HPS6):c.2181A>G (p.Ala727=) rs199518658
NM_024747.5(HPS6):c.2231G>T (p.Gly744Val) rs770148492
NM_024747.5(HPS6):c.2307G>A (p.Pro769=) rs553794194
NM_024747.5(HPS6):c.238dup (p.Asp80fs) rs281865108
NM_024747.5(HPS6):c.298C>T (p.Leu100=) rs886046650
NM_024747.5(HPS6):c.337C>T (p.Arg113Trp) rs371307947
NM_024747.5(HPS6):c.541A>G (p.Thr181Ala) rs144257610
NM_024747.5(HPS6):c.727C>A (p.Pro243Thr) rs767667481
NM_024747.6(HPS6):c.-5G>A
NM_024747.6(HPS6):c.1035G>A (p.Arg345=)
NM_024747.6(HPS6):c.1127G>A (p.Arg376His)
NM_024747.6(HPS6):c.1152T>C (p.Phe384=)
NM_024747.6(HPS6):c.1253G>T (p.Gly418Val)
NM_024747.6(HPS6):c.1346C>G (p.Ser449Cys)
NM_024747.6(HPS6):c.1363T>C (p.Leu455=)
NM_024747.6(HPS6):c.1430A>C (p.Asp477Ala)
NM_024747.6(HPS6):c.1679G>T (p.Gly560Val)
NM_024747.6(HPS6):c.1692C>A (p.Pro564=)
NM_024747.6(HPS6):c.1755G>T (p.Glu585Asp)
NM_024747.6(HPS6):c.1810C>G (p.Leu604Val)
NM_024747.6(HPS6):c.1951C>T (p.Arg651Trp)
NM_024747.6(HPS6):c.2045G>A (p.Arg682His)
NM_024747.6(HPS6):c.2112C>T (p.Leu704=)
NM_024747.6(HPS6):c.2166C>T (p.Phe722=)
NM_024747.6(HPS6):c.2254C>A (p.Pro752Thr)
NM_024747.6(HPS6):c.2323C>G (p.Leu775Val)
NM_024747.6(HPS6):c.277G>T (p.Val93Leu)
NM_024747.6(HPS6):c.303C>T (p.Ala101=)
NM_024747.6(HPS6):c.634G>A (p.Val212Met)
NM_024747.6(HPS6):c.732A>G (p.Gly244=)
NM_024747.6(HPS6):c.831C>G (p.Pro277=)

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