ClinVar Miner

List of variants in gene GNAO1 reported as uncertain significance by GeneDx

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_020988.3(GNAO1):c.275G>A (p.Gly92Asp) rs1271540719 0.00002
NM_020988.3(GNAO1):c.768C>T (p.Asn256=) rs779411534 0.00002
NM_020988.3(GNAO1):c.1015G>A (p.Val339Ile) rs2037954591 0.00001
NM_020988.3(GNAO1):c.256C>T (p.Arg86Trp) rs767115578 0.00001
NM_020988.3(GNAO1):c.284A>G (p.Tyr95Cys) rs1341492901 0.00001
NM_020988.3(GNAO1):c.428G>A (p.Arg143Gln) rs777414554 0.00001
NM_020988.3(GNAO1):c.54G>A (p.Ala18=) rs1288429932 0.00001
NM_020988.3(GNAO1):c.884A>G (p.Asn295Ser) rs371362351 0.00001
NM_020988.3(GNAO1):c.107T>C (p.Leu36Ser)
NM_020988.3(GNAO1):c.145A>C (p.Ile49Leu) rs763223472
NM_020988.3(GNAO1):c.158T>A (p.Met53Lys) rs2143272295
NM_020988.3(GNAO1):c.172G>A (p.Glu58Lys)
NM_020988.3(GNAO1):c.262A>G (p.Met88Val) rs1555504233
NM_020988.3(GNAO1):c.263T>C (p.Met88Thr)
NM_020988.3(GNAO1):c.290A>G (p.Asp97Gly) rs778669032
NM_020988.3(GNAO1):c.320T>C (p.Val107Ala)
NM_020988.3(GNAO1):c.326A>T (p.Asp109Val) rs2037659126
NM_020988.3(GNAO1):c.358T>G (p.Phe120Val) rs2037659527
NM_020988.3(GNAO1):c.463T>C (p.Tyr155His)
NM_020988.3(GNAO1):c.529C>T (p.Arg177Ter) rs2037724762
NM_020988.3(GNAO1):c.530G>A (p.Arg177Gln) rs2506872117
NM_020988.3(GNAO1):c.594G>T (p.Arg198Ser) rs2506876581
NM_020988.3(GNAO1):c.604G>A (p.Val202Ile) rs1297388989
NM_020988.3(GNAO1):c.614A>T (p.Gln205Leu) rs2143664881
NM_020988.3(GNAO1):c.617G>A (p.Arg206Gln) rs1297225571
NM_020988.3(GNAO1):c.641A>G (p.His214Arg)
NM_020988.3(GNAO1):c.694G>A (p.Asp232Asn) rs2506877012
NM_020988.3(GNAO1):c.723+4073T>C
NM_020988.3(GNAO1):c.723+4098C>A rs763864033
NM_020988.3(GNAO1):c.728G>A (p.Arg243His) rs2543427158
NM_020988.3(GNAO1):c.789C>G (p.Thr263=) rs1265902011
NM_020988.3(GNAO1):c.860G>A (p.Cys287Tyr) rs2543427382
NM_020988.3(GNAO1):c.865C>G (p.Pro289Ala)
NM_020988.3(GNAO1):c.929G>A (p.Ser310Asn)
NM_020988.3(GNAO1):c.986C>T (p.Thr329Met) rs2543432069

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