ClinVar Miner

List of variants in gene YWHAG reported as uncertain significance for not provided

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_012479.4(YWHAG):c.295G>A (p.Asp99Asn) rs759611694 0.00006
NM_012479.4(YWHAG):c.434C>T (p.Thr145Met) rs773949985 0.00001
NM_012479.4(YWHAG):c.475G>A (p.Glu159Lys) rs746119956 0.00001
NC_000007.13:g.(?_75958894)_(75959570_?)del
NC_000007.13:g.(?_75958894)_(75959570_?)dup
NC_000007.13:g.(?_75988019)_(75988125_?)dup
NM_012479.4(YWHAG):c.113C>T (p.Ser38Leu)
NM_012479.4(YWHAG):c.116A>T (p.Asn39Ile) rs2115589180
NM_012479.4(YWHAG):c.119A>C (p.Glu40Ala) rs2115589170
NM_012479.4(YWHAG):c.131T>G (p.Leu44Arg) rs2115589139
NM_012479.4(YWHAG):c.146A>C (p.Tyr49Ser)
NM_012479.4(YWHAG):c.160G>A (p.Gly54Arg)
NM_012479.4(YWHAG):c.163G>A (p.Ala55Thr) rs866370817
NM_012479.4(YWHAG):c.183_194del (p.Arg61_Ser64del) rs2115589017
NM_012479.4(YWHAG):c.19C>G (p.Leu7Val) rs1804004771
NM_012479.4(YWHAG):c.1A>G (p.Met1Val)
NM_012479.4(YWHAG):c.247C>G (p.Arg83Gly)
NM_012479.4(YWHAG):c.247C>T (p.Arg83Cys)
NM_012479.4(YWHAG):c.251C>T (p.Ala84Val)
NM_012479.4(YWHAG):c.256C>G (p.Arg86Gly)
NM_012479.4(YWHAG):c.256C>T (p.Arg86Trp)
NM_012479.4(YWHAG):c.257G>A (p.Arg86Gln)
NM_012479.4(YWHAG):c.259G>A (p.Glu87Lys)
NM_012479.4(YWHAG):c.279G>C (p.Leu93Phe) rs2115588825
NM_012479.4(YWHAG):c.301C>G (p.Leu101Val)
NM_012479.4(YWHAG):c.317A>G (p.Asn106Ser)
NM_012479.4(YWHAG):c.32C>G (p.Ala11Gly)
NM_012479.4(YWHAG):c.349T>A (p.Tyr117Asn)
NM_012479.4(YWHAG):c.383_385dup (p.Gly128_Asp129insGly)
NM_012479.4(YWHAG):c.383_388dup (p.Asp129_Tyr130insTrpAsp) rs2115588555
NM_012479.4(YWHAG):c.418G>A (p.Gly140Arg)
NM_012479.4(YWHAG):c.425A>G (p.Lys142Arg)
NM_012479.4(YWHAG):c.430G>A (p.Ala144Thr)
NM_012479.4(YWHAG):c.43G>A (p.Glu15Lys) rs2115667108
NM_012479.4(YWHAG):c.455A>G (p.Lys152Arg) rs2115588284
NM_012479.4(YWHAG):c.491A>G (p.His164Arg)
NM_012479.4(YWHAG):c.493dup (p.Met165fs)
NM_012479.4(YWHAG):c.511A>G (p.Ile171Val)
NM_012479.4(YWHAG):c.524T>C (p.Leu175Pro) rs2115588022
NM_012479.4(YWHAG):c.541G>A (p.Val181Ile)
NM_012479.4(YWHAG):c.560A>T (p.Gln187Leu)
NM_012479.4(YWHAG):c.565G>C (p.Ala189Pro)
NM_012479.4(YWHAG):c.566C>A (p.Ala189Asp)
NM_012479.4(YWHAG):c.578C>T (p.Ala193Val)
NM_012479.4(YWHAG):c.583C>T (p.His195Tyr)
NM_012479.4(YWHAG):c.599C>T (p.Ala200Val)
NM_012479.4(YWHAG):c.604G>C (p.Asp202His)
NM_012479.4(YWHAG):c.607G>A (p.Asp203Asn)
NM_012479.4(YWHAG):c.616G>A (p.Ala206Thr)
NM_012479.4(YWHAG):c.634_645del (p.Asn212_Ser215del)
NM_012479.4(YWHAG):c.63C>G (p.Asp21Glu)
NM_012479.4(YWHAG):c.648C>A (p.Tyr216Ter) rs2115587495
NM_012479.4(YWHAG):c.64G>A (p.Asp22Asn)
NM_012479.4(YWHAG):c.65A>G (p.Asp22Gly)
NM_012479.4(YWHAG):c.661C>T (p.Leu221Phe)
NM_012479.4(YWHAG):c.662T>G (p.Leu221Arg)
NM_012479.4(YWHAG):c.687C>A (p.Asn229Lys)
NM_012479.4(YWHAG):c.71C>T (p.Ala24Val)
NM_012479.4(YWHAG):c.7G>A (p.Asp3Asn)
NM_012479.4(YWHAG):c.80T>G (p.Met27Arg) rs2115666932

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