ClinVar Miner

List of variants reported as likely benign for Brunner syndrome

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000240.4(MAOA):c.1375-17T>C rs368285679 0.00050
NM_000240.4(MAOA):c.1526C>T (p.Thr509Ile) rs147298607 0.00034
NM_000240.4(MAOA):c.1437+14C>T rs372158657 0.00020
NM_000240.4(MAOA):c.412-6C>G rs369122751 0.00011
NM_000240.4(MAOA):c.1262+6A>G rs765738971 0.00010
NM_000240.4(MAOA):c.1119C>A (p.Ile373=) rs200913136 0.00006
NM_000240.4(MAOA):c.1389C>T (p.Leu463=) rs771568228 0.00006
NM_000240.4(MAOA):c.412-13C>T rs763906089 0.00006
NM_000240.4(MAOA):c.1262+19G>A rs377168294 0.00005
NM_000240.4(MAOA):c.1262+18C>T rs372784589 0.00004
NM_000240.4(MAOA):c.702C>T (p.Leu234=) rs370853887 0.00004
NM_000240.4(MAOA):c.956-8T>G rs780408416 0.00003
NM_000240.4(MAOA):c.1052+14G>A rs113551306 0.00002
NM_000240.4(MAOA):c.1262+7C>T rs773216160 0.00002
NM_000240.4(MAOA):c.255C>G (p.Gly85=) rs1601935224 0.00002
NM_000240.4(MAOA):c.30G>A (p.Ala10=) rs1347324620 0.00002
NM_000240.4(MAOA):c.681C>T (p.Ser227=) rs758225239 0.00002
NM_000240.4(MAOA):c.1165-11C>T rs948692153 0.00001
NM_000240.4(MAOA):c.1488C>G (p.Pro496=) rs1569203097 0.00001
NM_000240.4(MAOA):c.1545G>T (p.Gly515=) rs1223537199 0.00001
NM_000240.4(MAOA):c.1052+17T>G
NM_000240.4(MAOA):c.1053-10C>G rs1601948966
NM_000240.4(MAOA):c.1106+15C>T
NM_000240.4(MAOA):c.1164+7A>C
NM_000240.4(MAOA):c.1215C>T (p.Gly405=)
NM_000240.4(MAOA):c.1299G>A (p.Ala433=)
NM_000240.4(MAOA):c.1375-14T>C
NM_000240.4(MAOA):c.1401C>T (p.Thr467=)
NM_000240.4(MAOA):c.1437+11T>C
NM_000240.4(MAOA):c.1449G>A (p.Ala483=)
NM_000240.4(MAOA):c.15G>A (p.Glu5=) rs2147066663
NM_000240.4(MAOA):c.186C>T (p.Tyr62=)
NM_000240.4(MAOA):c.306+18C>A
NM_000240.4(MAOA):c.307-18T>C
NM_000240.4(MAOA):c.307-19G>C
NM_000240.4(MAOA):c.412-20G>A
NM_000240.4(MAOA):c.576G>T (p.Leu192=)
NM_000240.4(MAOA):c.73+19G>C
NM_000240.4(MAOA):c.732C>T (p.Val244=) rs980804164
NM_000240.4(MAOA):c.74-6C>T rs1196492976
NM_000240.4(MAOA):c.74-9T>A
NM_000240.4(MAOA):c.774G>A (p.Thr258=)
NM_000240.4(MAOA):c.796-15T>G
NM_000240.4(MAOA):c.796-9G>A rs2033882536
NM_000240.4(MAOA):c.804C>T (p.Tyr268=)
NM_000240.4(MAOA):c.831G>A (p.Leu277=)
NM_000240.4(MAOA):c.933G>A (p.Lys311=)

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