ClinVar Miner

List of variants in gene PLEKHG5 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NC_000001.11:g.6497544C>T
NC_000001.11:g.6497563C>G
NC_000001.11:g.6519593G>C
NC_000001.11:g.6519783C>T
NC_000001.11:g.6520176G>C
NC_000001.11:g.6520190C>T
NC_000001.11:g.6520337C>T
NC_000001.11:g.6520369C>T
NM_020631.4(PLEKHG5):c.-27998G>A rs1556035
NM_020631.4(PLEKHG5):c.-5400T>G rs3007430
NM_020631.5(PLEKHG5):c.-87-95_-87-94insATCCATTAGGGAGAGCTGGCCCAGGTCGGAGC
NM_020631.5(PLEKHG5):c.-88+1192G>A rs11806429
NM_020631.5(PLEKHG5):c.-88+5868C>G
NM_020631.5(PLEKHG5):c.-88+5G>A rs3007429
NM_020631.5(PLEKHG5):c.-88+6307T>A rs75490131
NM_020631.5(PLEKHG5):c.1282-111T>C
NM_020631.5(PLEKHG5):c.1393-24dup
NM_020631.5(PLEKHG5):c.1800+107C>T
NM_020631.5(PLEKHG5):c.2145_2147GGA[7] (p.Glu723del) rs113541584
NM_020631.5(PLEKHG5):c.2319C>T (p.Pro773=) rs80031446
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.3012-113G>A
NM_020631.5(PLEKHG5):c.302+176T>C
NM_020631.5(PLEKHG5):c.303-134C>T
NM_020631.5(PLEKHG5):c.30C>T (p.Asp10=) rs114209691
NM_020631.5(PLEKHG5):c.440-6A>G rs202049535
NM_020631.5(PLEKHG5):c.495G>A (p.Lys165=) rs150772386
NM_020631.5(PLEKHG5):c.591+28G>C
NM_020631.5(PLEKHG5):c.591+52G>A
NM_020631.5(PLEKHG5):c.591+71G>A
NM_020631.5(PLEKHG5):c.592-14C>T rs554879611
NM_020631.5(PLEKHG5):c.795+8G>A rs114275646
NM_020631.5(PLEKHG5):c.88C>T (p.Arg30Cys) rs111400494
NM_020631.5(PLEKHG5):c.918C>T (p.Asp306=) rs111624565

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