ClinVar Miner

List of variants in gene HTRA1 reported as likely benign for not provided

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Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_002775.5(HTRA1):c.778-20G>A rs74159166 0.04347
NM_002775.5(HTRA1):c.753C>T (p.Ile251=) rs17624021 0.04155
NM_002775.5(HTRA1):c.337G>T (p.Ala113Ser) rs140088745 0.00485
NM_002775.5(HTRA1):c.1221C>T (p.Asp407=) rs11538140 0.00305
NM_002775.5(HTRA1):c.879C>T (p.Thr293=) rs149294320 0.00207
NM_002775.5(HTRA1):c.1094C>T (p.Thr365Met) rs139620409 0.00056
NM_002775.5(HTRA1):c.415T>G (p.Ser139Ala) rs530087850 0.00031
NM_002775.5(HTRA1):c.1323C>T (p.Ser441=) rs111580234 0.00026
NM_002775.5(HTRA1):c.12G>T (p.Pro4=) rs761008513 0.00021
NM_002775.5(HTRA1):c.1065C>T (p.Ile355=) rs371612872 0.00019
NM_002775.5(HTRA1):c.176G>C (p.Arg59Pro) rs1246114252 0.00012
NM_002775.5(HTRA1):c.472+6C>A rs550039968 0.00012
NM_002775.5(HTRA1):c.165C>A (p.Gly55=) rs947247701 0.00009
NM_002775.5(HTRA1):c.1008C>T (p.Asp336=) rs768614813 0.00007
NM_002775.5(HTRA1):c.1350C>T (p.Asp450=) rs374675648 0.00007
NM_002775.5(HTRA1):c.1121-13G>A rs138859679 0.00006
NM_002775.5(HTRA1):c.843C>T (p.Ala281=) rs202167109 0.00006
NM_002775.5(HTRA1):c.15C>G (p.Arg5=) rs900233098 0.00005
NM_002775.5(HTRA1):c.1173G>A (p.Thr391=) rs761057470 0.00004
NM_002775.5(HTRA1):c.1296C>T (p.Asp432=) rs368158443 0.00004
NM_002775.5(HTRA1):c.144G>T (p.Pro48=) rs565162637 0.00004
NM_002775.5(HTRA1):c.957C>T (p.Thr319=) rs373287445 0.00003
NM_002775.5(HTRA1):c.973-6T>C rs747305348 0.00002
NM_002775.5(HTRA1):c.1389C>T (p.Arg463=) rs1289545540 0.00001
NM_002775.5(HTRA1):c.1413C>T (p.Ile471=) rs1233591873 0.00001
NM_002775.5(HTRA1):c.1425C>T (p.Pro475=) rs779158785 0.00001
NM_002775.5(HTRA1):c.573-8G>A rs779261850 0.00001
NM_002775.5(HTRA1):c.579G>A (p.Pro193=) rs772327746 0.00001
NM_002775.5(HTRA1):c.603G>A (p.Val201=) rs201878826 0.00001
NM_002775.5(HTRA1):c.846C>T (p.Ile282=) rs754351568 0.00001
NM_002775.5(HTRA1):c.973-7A>T rs778011757 0.00001
NM_002775.5(HTRA1):c.1011T>C (p.Gly337=)
NM_002775.5(HTRA1):c.1086G>A (p.Lys362=)
NM_002775.5(HTRA1):c.1095G>C (p.Thr365=) rs752097769
NM_002775.5(HTRA1):c.1134C>T (p.Thr378=)
NM_002775.5(HTRA1):c.1152T>C (p.Gly384=)
NM_002775.5(HTRA1):c.1158A>C (p.Arg386=)
NM_002775.5(HTRA1):c.1178+12G>A
NM_002775.5(HTRA1):c.1178+17C>T
NM_002775.5(HTRA1):c.1207C>T (p.Arg403Trp)
NM_002775.5(HTRA1):c.1230A>C (p.Ser410=)
NM_002775.5(HTRA1):c.123C>T (p.Cys41=)
NM_002775.5(HTRA1):c.1254T>C (p.Ile418=)
NM_002775.5(HTRA1):c.126G>A (p.Glu42=) rs2133905058
NM_002775.5(HTRA1):c.1275-9G>A
NM_002775.5(HTRA1):c.1314T>C (p.Asn438=) rs2133454695
NM_002775.5(HTRA1):c.1332C>T (p.Ser444=)
NM_002775.5(HTRA1):c.1347C>T (p.Ser449=)
NM_002775.5(HTRA1):c.1416A>T (p.Thr472=) rs1402889573
NM_002775.5(HTRA1):c.150G>A (p.Pro50=)
NM_002775.5(HTRA1):c.180C>T (p.Asp60=) rs1259285601
NM_002775.5(HTRA1):c.204C>T (p.Cys68=)
NM_002775.5(HTRA1):c.246G>C (p.Pro82=)
NM_002775.5(HTRA1):c.300G>A (p.Thr100=)
NM_002775.5(HTRA1):c.327C>G (p.Leu109=)
NM_002775.5(HTRA1):c.33_34insTCC (p.Leu11_Leu12insSer) rs541533723
NM_002775.5(HTRA1):c.34C>T (p.Leu12=) rs996483189
NM_002775.5(HTRA1):c.351G>T (p.Pro117=) rs765344403
NM_002775.5(HTRA1):c.417C>G (p.Ser139=)
NM_002775.5(HTRA1):c.465C>T (p.Cys155=) rs1591022118
NM_002775.5(HTRA1):c.473-13C>A
NM_002775.5(HTRA1):c.504A>G (p.Lys168=)
NM_002775.5(HTRA1):c.540C>T (p.Ala180=)
NM_002775.5(HTRA1):c.546C>T (p.Ala182=)
NM_002775.5(HTRA1):c.572+12C>T
NM_002775.5(HTRA1):c.624T>C (p.Ile208=)
NM_002775.5(HTRA1):c.645C>T (p.Ile215=)
NM_002775.5(HTRA1):c.672C>T (p.Asn224=) rs756634374
NM_002775.5(HTRA1):c.702C>T (p.Asn234=)
NM_002775.5(HTRA1):c.70C>T (p.Leu24=)
NM_002775.5(HTRA1):c.756A>G (p.Ala252=)
NM_002775.5(HTRA1):c.777+17C>T
NM_002775.5(HTRA1):c.778-15C>T
NM_002775.5(HTRA1):c.778-7G>A
NM_002775.5(HTRA1):c.84C>A (p.Gly28=)
NM_002775.5(HTRA1):c.879C>A (p.Thr293=)
NM_002775.5(HTRA1):c.909C>T (p.Gly303=)
NM_002775.5(HTRA1):c.96T>G (p.Pro32=) rs779504282
NM_002775.5(HTRA1):c.973-18A>G
NM_002775.5(HTRA1):c.973-20T>A
NM_002775.5(HTRA1):c.990C>A (p.Gly330=)
NM_002775.5(HTRA1):c.9C>A (p.Ile3=)

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