List of variants reported as likely pathogenic for Mental retardation, X-linked, syndromic, Turner type

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Total variants: 17

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HGVS	dbSNP
NM_031407.7(HUWE1):c.12067C>T (p.Arg4023Cys)	rs1556914274
NM_031407.7(HUWE1):c.12205A>T (p.Ile4069Phe)	rs1556913268
NM_031407.7(HUWE1):c.12225C>G (p.Asn4075Lys)	rs1556913258
NM_031407.7(HUWE1):c.12317A>G (p.Tyr4106Cys)	rs1556913180
NM_031407.7(HUWE1):c.12469C>G (p.Leu4157Val)	rs1556912828
NM_031407.7(HUWE1):c.12732G>C (p.Glu4244Asp)	rs1556910184
NM_031407.7(HUWE1):c.12885G>C (p.Lys4295Asn)	rs1325394060
NM_031407.7(HUWE1):c.1978G>A (p.Gly660Arg)	rs1557006903
NM_031407.7(HUWE1):c.2007T>G (p.His669Gln)	rs1557006873
NM_031407.7(HUWE1):c.3239G>A (p.Arg1080His)	rs1057518704
NM_031407.7(HUWE1):c.344C>T (p.Ser115Phe)	rs1557036757
NM_031407.7(HUWE1):c.3982A>G (p.Met1328Val)	rs1556978515
NM_031407.7(HUWE1):c.4013C>T (p.Ala1338Val)	rs863224879
NM_031407.7(HUWE1):c.6098-20_6109del	rs1602738933
NM_031407.7(HUWE1):c.6267T>G (p.Ile2089Met)	rs1556955128
NM_031407.7(HUWE1):c.9208C>T (p.Arg3070Cys)	rs886041876
NM_031407.7(HUWE1):c.9581T>C (p.Phe3194Ser)	rs782393002

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