ClinVar Miner

List of variants in gene PLEKHG5 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_003790.2(TNFRSF25):c.-77_-74del rs45542640
NM_020631.5(PLEKHG5):c.*1052G>A rs148036862
NM_020631.5(PLEKHG5):c.*108G>A rs11800788
NM_020631.5(PLEKHG5):c.*1158G>C rs2986754
NM_020631.5(PLEKHG5):c.*1304G>A rs45604837
NM_020631.5(PLEKHG5):c.*1313C>T rs45574533
NM_020631.5(PLEKHG5):c.*27T>C rs117494970
NM_020631.5(PLEKHG5):c.*290T>C rs14708
NM_020631.5(PLEKHG5):c.*697C>T rs3176900
NM_020631.5(PLEKHG5):c.*765T>A rs538175057
NM_020631.5(PLEKHG5):c.*843G>T rs12735472
NM_020631.5(PLEKHG5):c.*990C>T rs3007418
NM_020631.5(PLEKHG5):c.-88+5G>A rs3007429
NM_020631.5(PLEKHG5):c.1179G>A (p.Leu393=) rs112471131
NM_020631.5(PLEKHG5):c.1240G>A (p.Ala414Thr) rs74809741
NM_020631.5(PLEKHG5):c.1318A>G (p.Met440Val) rs61740145
NM_020631.5(PLEKHG5):c.1801-12C>A rs943584
NM_020631.5(PLEKHG5):c.2001T>C (p.Ser667=) rs730600
NM_020631.5(PLEKHG5):c.2163G>A (p.Glu721=) rs62639695
NM_020631.5(PLEKHG5):c.2307G>A (p.Thr769=) rs3138150
NM_020631.5(PLEKHG5):c.2331C>T (p.Ser777=) rs61749272
NM_020631.5(PLEKHG5):c.2428G>A (p.Gly810Ser) rs76625876
NM_020631.5(PLEKHG5):c.2576G>A (p.Arg859His) rs61737997
NM_020631.5(PLEKHG5):c.2581C>T (p.Arg861Cys) rs148560273
NM_020631.5(PLEKHG5):c.2594A>G (p.Gln865Arg) rs3007419
NM_020631.5(PLEKHG5):c.260T>C (p.Ile87Thr) rs117505788
NM_020631.5(PLEKHG5):c.2827G>C (p.Gly943Arg) rs114619322
NM_020631.5(PLEKHG5):c.30C>T (p.Asp10=) rs114209691
NM_020631.5(PLEKHG5):c.43+13G>A rs78593902
NM_020631.5(PLEKHG5):c.440-6A>G rs202049535
NM_020631.5(PLEKHG5):c.495G>A (p.Lys165=) rs150772386
NM_020631.5(PLEKHG5):c.691G>A (p.Gly231Ser) rs146651455
NM_020631.5(PLEKHG5):c.713C>G (p.Thr238Ser) rs61741379
NM_020631.5(PLEKHG5):c.795+8G>A rs114275646
NM_020631.6(PLEKHG5):c.*63C>T

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