ClinVar Miner

List of variants in gene PLEKHG5 reported as likely benign for not provided

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_001265594.2(PLEKHG5):c.2737+22_2737+24del rs536097668
NM_020631.5(PLEKHG5):c.1080+131G>A rs75624694
NM_020631.5(PLEKHG5):c.1132-6G>C rs1569860714
NM_020631.5(PLEKHG5):c.12T>C (p.Asp4=) rs772435791
NM_020631.5(PLEKHG5):c.1392+40G>C rs181693536
NM_020631.5(PLEKHG5):c.1443G>A (p.Leu481=) rs1175716993
NM_020631.5(PLEKHG5):c.1530C>T (p.Ala510=) rs61734080
NM_020631.5(PLEKHG5):c.1572C>T (p.His524=) rs373184968
NM_020631.5(PLEKHG5):c.1635C>T (p.Ile545=) rs1569851488
NM_020631.5(PLEKHG5):c.1935G>A (p.Gly645=) rs147140763
NM_020631.5(PLEKHG5):c.2235C>T (p.Pro745=) rs1323858843
NM_020631.5(PLEKHG5):c.2244G>A (p.Gln748=) rs1569839599
NM_020631.5(PLEKHG5):c.2361C>T (p.Thr787=) rs201054338
NM_020631.5(PLEKHG5):c.2598G>A (p.Leu866=) rs368328495
NM_020631.5(PLEKHG5):c.2610G>A (p.Pro870=) rs373880458
NM_020631.5(PLEKHG5):c.2676T>C (p.His892=) rs758308121
NM_020631.5(PLEKHG5):c.2811C>T (p.Ser937=) rs1232546435
NM_020631.5(PLEKHG5):c.2826C>T (p.Val942=) rs749891873
NM_020631.5(PLEKHG5):c.3012-79C>T rs78137382
NM_020631.5(PLEKHG5):c.33T>C (p.Leu11=) rs144859183
NM_020631.5(PLEKHG5):c.534G>T (p.Gly178=) rs1569875832
NM_020631.5(PLEKHG5):c.592-75C>A rs140246821
NM_020631.5(PLEKHG5):c.594C>G (p.Ala198=) rs1557745612
NM_020631.5(PLEKHG5):c.777C>T (p.Ser259=) rs373244537
NM_020631.5(PLEKHG5):c.834C>T (p.His278=) rs368463952
NM_020631.5(PLEKHG5):c.84G>A (p.Pro28=) rs140428005
NM_020631.5(PLEKHG5):c.87G>A (p.Pro29=) rs140892576
NM_020631.5(PLEKHG5):c.903G>A (p.Glu301=) rs780277728
NM_020631.5(PLEKHG5):c.997C>A (p.Arg333=) rs148232621
NM_198681.4(PLEKHG5):c.-164-200C>G rs145275535
NM_198681.4(PLEKHG5):c.-164-831T>C rs549207658
NM_198681.4(PLEKHG5):c.-181C>G rs17438786

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