ClinVar Miner

List of variants in gene DAG1 reported as likely benign for not provided

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Total variants: 35
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HGVS dbSNP gnomAD frequency
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.-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.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.1212G>A (p.Thr404=) rs139781017 0.00051
NM_004393.6(DAG1):c.1022C>T (p.Thr341Ile) rs148759919 0.00048
NM_004393.6(DAG1):c.1308G>A (p.Thr436=) rs143763229 0.00017
NM_004393.6(DAG1):c.286-10del rs747305463 0.00012
NM_004393.6(DAG1):c.183T>C (p.Val61=) rs775928044 0.00007
NM_004393.6(DAG1):c.1690C>A (p.Leu564Ile) rs199894361 0.00006
NM_004393.6(DAG1):c.510C>A (p.Ala170=) rs147153370 0.00006
NM_004393.6(DAG1):c.735G>A (p.Pro245=) rs748164001 0.00006
NM_004393.6(DAG1):c.927C>T (p.Arg309=) rs551679833 0.00006
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.1014C>T (p.Ile338=) rs773685771 0.00001
NM_004393.6(DAG1):c.1230T>C (p.Tyr410=) rs374625327 0.00001
NM_004393.6(DAG1):c.1785C>T (p.Val595=) rs762148188 0.00001
NM_004393.6(DAG1):c.-116-4dup rs200455639
NM_004393.6(DAG1):c.-24G>T rs750907019
NM_004393.6(DAG1):c.1149C>A (p.Gly383=)
NM_004393.6(DAG1):c.1858T>C (p.Leu620=) rs1466654266
NM_004393.6(DAG1):c.2190G>A (p.Glu730=) rs1293129309
NM_004393.6(DAG1):c.2343C>G (p.Gly781=) rs1575414093
NM_004393.6(DAG1):c.261T>C (p.Ile87=) rs1575387362
NM_004393.6(DAG1):c.631C>T (p.Leu211=)

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