ClinVar Miner

List of variants in gene DAG1 reported by GeneDx

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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_004393.6(DAG1):c.285+42T>C rs2329024 0.97521
NM_001177643.2(DAG1):c.-306C>T rs6797164 0.97426
NM_004393.6(DAG1):c.286-135G>A rs2311801 0.97418
NM_004393.6(DAG1):c.-117+18178A>T rs4855860 0.89930
NM_004393.6(DAG1):c.-117+18434C>T rs4855859 0.39967
NM_004393.6(DAG1):c.-117+18096G>T rs4855861 0.39847
NM_004393.6(DAG1):c.*250T>C rs1050088 0.39364
NM_004393.6(DAG1):c.-117+17230A>G rs9818590 0.31361
NM_004393.6(DAG1):c.2256C>T (p.His752=) rs1801143 0.30176
NM_004393.6(DAG1):c.-117+18092T>C rs11719996 0.29199
NM_004393.6(DAG1):c.-116-291T>C rs7622302 0.28264
NM_004393.6(DAG1):c.-117+16912G>C rs6783003 0.20241
NM_004393.6(DAG1):c.286-49G>A rs115435316 0.02085
NM_004393.6(DAG1):c.286-333G>C rs79896705 0.01286
NM_004393.6(DAG1):c.-117+6669A>G rs139212261 0.00960
NM_004393.6(DAG1):c.2231G>C (p.Ser744Thr) rs114357468 0.00947
NM_004393.6(DAG1):c.2271C>T (p.Ala757=) rs78281659 0.00786
NM_004393.6(DAG1):c.-117+18178del rs200848559 0.00675
NM_004393.6(DAG1):c.259A>G (p.Ile87Val) rs116717961 0.00640
NM_004393.6(DAG1):c.*294G>T rs140844035 0.00548
NM_004393.6(DAG1):c.1701C>T (p.Ser567=) rs142579425 0.00456
NM_004393.6(DAG1):c.258G>C (p.Leu86Phe) rs145403829 0.00314
NM_004393.6(DAG1):c.1233G>A (p.Val411=) rs145765079 0.00249
NM_004393.6(DAG1):c.2036G>A (p.Arg679His) rs113904914 0.00227
NM_004393.6(DAG1):c.599C>G (p.Thr200Ser) rs41290704 0.00167
NM_004393.6(DAG1):c.278T>C (p.Ile93Thr) rs149218670 0.00106
NM_004393.6(DAG1):c.2082C>T (p.Asn694=) rs146453412 0.00091
NM_004393.6(DAG1):c.2520T>C (p.Thr840=) rs149564053 0.00074
NM_004393.6(DAG1):c.331G>A (p.Asp111Asn) rs117209107 0.00072
NM_004393.6(DAG1):c.1212G>A (p.Thr404=) rs139781017 0.00051
NM_004393.6(DAG1):c.1022C>T (p.Thr341Ile) rs148759919 0.00048
NM_004393.6(DAG1):c.920C>G (p.Pro307Arg) rs374092106 0.00024
NM_004393.6(DAG1):c.1308G>A (p.Thr436=) rs143763229 0.00017
NM_004393.6(DAG1):c.1719C>T (p.His573=) rs146157416 0.00016
NM_004393.6(DAG1):c.286-10del rs747305463 0.00012
NM_004393.6(DAG1):c.1306A>G (p.Thr436Ala) rs149838438 0.00009
NM_004393.6(DAG1):c.-34C>T rs372102352 0.00006
NM_004393.6(DAG1):c.1690C>A (p.Leu564Ile) rs199894361 0.00006
NM_004393.6(DAG1):c.1708G>A (p.Val570Met) rs370669533 0.00006
NM_004393.6(DAG1):c.244A>G (p.Ile82Val) rs141706514 0.00006
NM_004393.6(DAG1):c.510C>A (p.Ala170=) rs147153370 0.00006
NM_004393.6(DAG1):c.829G>A (p.Val277Ile) rs375892170 0.00006
NM_004393.6(DAG1):c.927C>T (p.Arg309=) rs551679833 0.00006
NM_004393.6(DAG1):c.2406C>T (p.Asp802=) rs146134719 0.00005
NM_004393.6(DAG1):c.1283G>A (p.Arg428Gln) rs780793711 0.00004
NM_004393.6(DAG1):c.2123C>T (p.Thr708Met) rs758254304 0.00004
NM_004393.6(DAG1):c.222C>T (p.Val74=) rs150727558 0.00004
NM_004393.6(DAG1):c.243C>G (p.Thr81=) rs202047972 0.00004
NM_004393.6(DAG1):c.559C>T (p.Pro187Ser) rs145540662 0.00004
NM_004393.6(DAG1):c.213G>A (p.Thr71=) rs148703095 0.00003
NM_004393.6(DAG1):c.1186A>G (p.Thr396Ala) rs779846682 0.00002
NM_004393.6(DAG1):c.1210A>G (p.Thr404Ala) rs769229834 0.00002
NM_004393.6(DAG1):c.1674C>T (p.Ser558=) rs768293578 0.00001
NM_004393.6(DAG1):c.2610A>C (p.Thr870=) rs779926178 0.00001
NM_004393.6(DAG1):c.268A>C (p.Ser90Arg) rs140454570 0.00001
NM_001177643.2(DAG1):c.-320dup rs1553641460
NM_001177643.2(DAG1):c.-332dup rs71080520
NM_004393.6(DAG1):c.-116-4dup rs200455639
NM_004393.6(DAG1):c.-24G>T rs750907019
NM_004393.6(DAG1):c.1442G>C (p.Arg481Pro) rs1256677839
NM_004393.6(DAG1):c.1591_1593del (p.Thr531del) rs1553653146
NM_004393.6(DAG1):c.175G>T (p.Glu59Ter) rs767737417
NM_004393.6(DAG1):c.1771_1796del (p.Phe591fs) rs1064793360
NM_004393.6(DAG1):c.2270C>T (p.Ala757Val) rs1131691522
NM_004393.6(DAG1):c.2629G>A (p.Gly877Ser) rs2107959292
NM_004393.6(DAG1):c.310_311del (p.Leu104fs) rs1131691506
NM_004393.6(DAG1):c.384G>T (p.Val128=) rs143829263
NM_004393.6(DAG1):c.556G>T (p.Glu186Ter) rs1575410562
NM_004393.6(DAG1):c.891G>A (p.Trp297Ter) rs1553652751

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