ClinVar Miner

List of variants in gene VIPAS39 reported as uncertain significance by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001193315.2(VIPAS39):c.1455C>A (p.Ser485Arg) rs145453157 0.00129
NM_001193315.2(VIPAS39):c.1460C>T (p.Ser487Leu) rs140365206 0.00084
NM_001193315.2(VIPAS39):c.972C>T (p.Arg324=) rs147303718 0.00084
NM_001193315.2(VIPAS39):c.598-6C>G rs141155709 0.00081
NM_001193315.2(VIPAS39):c.447+9C>T rs145373891 0.00045
NM_001193315.2(VIPAS39):c.558A>G (p.Glu186=) rs148623263 0.00035
NM_001193315.2(VIPAS39):c.504+9A>G rs371762531 0.00028
NM_001193315.2(VIPAS39):c.1071C>T (p.Asn357=) rs138544284 0.00024
NM_001193315.2(VIPAS39):c.171C>G (p.Val57=) rs144120903 0.00023
NM_001193315.2(VIPAS39):c.1081A>G (p.Thr361Ala) rs201857750 0.00014
NM_001193315.2(VIPAS39):c.1254T>C (p.Asn418=) rs188105111 0.00008
NM_001193315.2(VIPAS39):c.78C>T (p.Asp26=) rs112217896 0.00007
NM_001193315.2(VIPAS39):c.1363C>T (p.Arg455Trp) rs149168488 0.00006
NM_001193315.2(VIPAS39):c.1393G>A (p.Ala465Thr) rs138274958 0.00005
NM_001193315.2(VIPAS39):c.1286A>G (p.Asn429Ser) rs763242224 0.00004
NM_001193315.2(VIPAS39):c.167G>A (p.Arg56Gln) rs146723692 0.00004
NM_001193315.2(VIPAS39):c.401C>T (p.Ala134Val) rs200635964 0.00004
NM_001193315.2(VIPAS39):c.527G>A (p.Arg176His) rs372813446 0.00004
NM_001193315.2(VIPAS39):c.632-9G>A rs370850533 0.00004
NM_001193315.2(VIPAS39):c.1089+8C>G rs371371767 0.00003
NM_001193315.2(VIPAS39):c.15G>A (p.Lys5=) rs768593671 0.00003
NM_001193315.2(VIPAS39):c.246C>T (p.His82=) rs569525220 0.00003
NM_001193315.2(VIPAS39):c.272G>A (p.Arg91Gln) rs188151618 0.00003
NM_001193315.2(VIPAS39):c.1005A>T (p.Thr335=) rs765454382 0.00002
NM_001193315.2(VIPAS39):c.1164C>T (p.Ala388=) rs886043868 0.00002
NM_001193315.2(VIPAS39):c.467G>A (p.Ser156Asn) rs754618039 0.00002
NM_001193315.2(VIPAS39):c.884C>T (p.Thr295Met) rs371894407 0.00002
NM_001193315.2(VIPAS39):c.1196C>T (p.Thr399Ile) rs377223868 0.00001
NM_001193315.2(VIPAS39):c.1221C>T (p.Phe407=) rs886044709 0.00001
NM_001193315.2(VIPAS39):c.1266+5T>C rs762123926 0.00001
NM_001193315.2(VIPAS39):c.1348G>A (p.Val450Ile) rs199989629 0.00001
NM_001193315.2(VIPAS39):c.1356+8C>T rs988006454 0.00001
NM_001193315.2(VIPAS39):c.344-8A>G rs970524687 0.00001
NM_001193315.2(VIPAS39):c.485G>A (p.Arg162Gln) rs144078420 0.00001
NM_001193315.2(VIPAS39):c.494G>A (p.Arg165Gln) rs376797384 0.00001
NM_001193315.2(VIPAS39):c.53A>G (p.Lys18Arg) rs745431826 0.00001
NM_001193315.2(VIPAS39):c.597+10C>T rs376603353 0.00001
NM_001193315.2(VIPAS39):c.70G>A (p.Asp24Asn) rs748505042 0.00001
NM_001193315.2(VIPAS39):c.110G>A (p.Arg37Gln) rs537717904
NM_001193315.2(VIPAS39):c.1199A>G (p.Lys400Arg) rs794727213
NM_001193315.2(VIPAS39):c.1226G>C (p.Arg409Pro) rs200598365
NM_001193315.2(VIPAS39):c.130G>T (p.Asp44Tyr) rs1023104472
NM_001193315.2(VIPAS39):c.1315A>G (p.Asn439Asp) rs1456890108
NM_001193315.2(VIPAS39):c.1365G>C (p.Arg455=) rs1566719540
NM_001193315.2(VIPAS39):c.1461+8G>T rs1566719337
NM_001193315.2(VIPAS39):c.235G>T (p.Gly79Cys) rs752936456
NM_001193315.2(VIPAS39):c.394A>T (p.Thr132Ser) rs1566736968
NM_001193315.2(VIPAS39):c.415C>T (p.Pro139Ser) rs763569201
NM_001193315.2(VIPAS39):c.461A>C (p.Asp154Ala) rs1566736255
NM_001193315.2(VIPAS39):c.479C>T (p.Thr160Ile) rs1555367578
NM_001193315.2(VIPAS39):c.505-4C>A rs1555366702
NM_001193315.2(VIPAS39):c.913-10T>C rs770890832
NM_001193315.2(VIPAS39):c.940G>C (p.Gly314Arg) rs757963657

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