ClinVar Miner

List of variants in gene combination ALDH5A1, GPLD1, LOC129995978 reported as likely benign

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_001080.3(ALDH5A1):c.10T>G (p.Cys4Gly) rs200793796 0.00760
NM_001080.3(ALDH5A1):c.130C>G (p.Leu44Val) rs185042766 0.00250
NM_001080.3(ALDH5A1):c.13A>G (p.Ile5Val) rs200398000 0.00096
NM_001080.3(ALDH5A1):c.183C>G (p.Thr61=) rs776791710 0.00057
NM_001080.3(ALDH5A1):c.175C>T (p.Leu59=) rs907112605 0.00032
NM_001080.3(ALDH5A1):c.62G>A (p.Gly21Asp) rs371923295 0.00016
NM_001080.3(ALDH5A1):c.123G>A (p.Pro41=) rs886042931 0.00009
NM_001080.3(ALDH5A1):c.18G>T (p.Trp6Cys) rs569456241 0.00009
NM_001080.3(ALDH5A1):c.12C>T (p.Cys4=) rs764183507 0.00007
NM_001080.3(ALDH5A1):c.188G>T (p.Ser63Ile) rs374908367 0.00007
NM_001080.3(ALDH5A1):c.32G>A (p.Gly11Glu) rs373315916 0.00007
NM_001080.3(ALDH5A1):c.22C>T (p.Arg8Trp) rs767601869 0.00004
NM_001080.3(ALDH5A1):c.162C>T (p.Leu54=) rs760612467 0.00003
NM_001080.3(ALDH5A1):c.51G>A (p.Ser17=) rs756763728 0.00002
NM_001080.3(ALDH5A1):c.75C>T (p.Arg25=) rs755799999 0.00002
NM_001080.3(ALDH5A1):c.120C>A (p.Gly40=) rs1764664599 0.00001
NM_001080.3(ALDH5A1):c.141C>T (p.Tyr47=) rs1182147990 0.00001
NM_001080.3(ALDH5A1):c.147G>T (p.Gly49=) rs1262777866 0.00001
NM_001080.3(ALDH5A1):c.153G>C (p.Leu51=) rs1164640012 0.00001
NM_001080.3(ALDH5A1):c.168G>C (p.Ala56=) rs371548862 0.00001
NM_001080.3(ALDH5A1):c.180C>T (p.Arg60=) rs1306264998 0.00001
NM_001080.3(ALDH5A1):c.186C>T (p.Asp62=) rs1346879524 0.00001
NM_001080.3(ALDH5A1):c.210C>T (p.Leu70=) rs1012047151 0.00001
NM_001080.3(ALDH5A1):c.213G>A (p.Pro71=) rs1220581277 0.00001
NM_001080.3(ALDH5A1):c.219C>A (p.Ala73=) rs1200016885 0.00001
NM_001080.3(ALDH5A1):c.21G>A (p.Leu7=) rs762014234 0.00001
NM_001080.3(ALDH5A1):c.231C>G (p.Pro77=) rs1160948222 0.00001
NM_001080.3(ALDH5A1):c.258T>C (p.Ala86=) rs1225985397 0.00001
NM_001080.3(ALDH5A1):c.291G>A (p.Glu97=) rs973569793 0.00001
NM_001080.3(ALDH5A1):c.54G>A (p.Thr18=) rs1254730579 0.00001
NM_001080.3(ALDH5A1):c.-9G>A rs2532810543
NM_001080.3(ALDH5A1):c.102C>G (p.Ala34=) rs779034609
NM_001080.3(ALDH5A1):c.105C>T (p.Ser35=) rs2532811413
NM_001080.3(ALDH5A1):c.108G>A (p.Gly36=)
NM_001080.3(ALDH5A1):c.109C>G (p.Pro37Ala) rs1764663348
NM_001080.3(ALDH5A1):c.117C>G (p.Pro39=) rs1261800997
NM_001080.3(ALDH5A1):c.117C>T (p.Pro39=) rs1261800997
NM_001080.3(ALDH5A1):c.120C>G (p.Gly40=)
NM_001080.3(ALDH5A1):c.126C>T (p.Ala42=) rs944589315
NM_001080.3(ALDH5A1):c.138C>T (p.Cys46=) rs1248918160
NM_001080.3(ALDH5A1):c.156G>C (p.Ala52=) rs1379009989
NM_001080.3(ALDH5A1):c.156G>T (p.Ala52=) rs1379009989
NM_001080.3(ALDH5A1):c.172C>T (p.Leu58=) rs2532812076
NM_001080.3(ALDH5A1):c.183C>A (p.Thr61=) rs776791710
NM_001080.3(ALDH5A1):c.183C>T (p.Thr61=) rs776791710
NM_001080.3(ALDH5A1):c.216C>T (p.Ala72=) rs1271075914
NM_001080.3(ALDH5A1):c.219C>T (p.Ala73=) rs1200016885
NM_001080.3(ALDH5A1):c.225C>A (p.Thr75=)
NM_001080.3(ALDH5A1):c.225C>T (p.Thr75=) rs1581800805
NM_001080.3(ALDH5A1):c.243G>C (p.Pro81=) rs1457060534
NM_001080.3(ALDH5A1):c.24G>C (p.Arg8=) rs1427888209
NM_001080.3(ALDH5A1):c.24G>T (p.Arg8=) rs1427888209
NM_001080.3(ALDH5A1):c.264C>A (p.Gly88=) rs759932020
NM_001080.3(ALDH5A1):c.264C>T (p.Gly88=) rs759932020
NM_001080.3(ALDH5A1):c.270A>T (p.Val90=) rs2127379071
NM_001080.3(ALDH5A1):c.273C>G (p.Ala91=) rs1206650969
NM_001080.3(ALDH5A1):c.282G>C (p.Gly94=)
NM_001080.3(ALDH5A1):c.288A>G (p.Arg96=) rs1554135737
NM_001080.3(ALDH5A1):c.42C>T (p.Arg14=) rs2127378795
NM_001080.3(ALDH5A1):c.54G>T (p.Thr18=) rs1254730579
NM_001080.3(ALDH5A1):c.60A>G (p.Pro20=)
NM_001080.3(ALDH5A1):c.63C>G (p.Gly21=) rs2532811083
NM_001080.3(ALDH5A1):c.75C>A (p.Arg25=) rs755799999
NM_001080.3(ALDH5A1):c.79C>G (p.Arg27Gly) rs779798309
NM_001080.3(ALDH5A1):c.87C>T (p.Gly29=) rs1581800500
NM_001080.3(ALDH5A1):c.93G>A (p.Leu31=)
NM_001080.3(ALDH5A1):c.93G>T (p.Leu31=) rs920257954

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