ClinVar Miner

List of variants in gene combination PRSS1, TRB reported as benign for Hereditary pancreatitis

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NC_000007.14:g.142749281A>C rs4726576 0.56847
NM_002769.5(PRSS1):c.738T>C (p.Asn246=) rs6667 0.53816
NM_002769.5(PRSS1):c.738= (p.Asn246=) rs6667 0.46184
NM_002769.5(PRSS1):c.592-79G>A rs531271210 0.00775
NM_002769.5(PRSS1):c.279C>T (p.Ile93=) rs139664510 0.00489
NM_002769.5(PRSS1):c.592-24C>T rs192452846 0.00354
NM_002769.5(PRSS1):c.592-11C>T rs183791770 0.00131
NM_002769.5(PRSS1):c.592-8C>T rs200381474 0.00131
NM_002769.5(PRSS1):c.40+10A>G rs199613498 0.00066
NM_002769.5(PRSS1):c.121C>T (p.Leu41=) rs369646357 0.00034
NM_002769.5(PRSS1):c.417C>T (p.Cys139=) rs141847266 0.00032
NM_002769.5(PRSS1):c.410C>T (p.Thr137Met) rs117497341 0.00024
NM_002769.5(PRSS1):c.623G>C (p.Gly208Ala) rs189270875 0.00024
NM_002769.5(PRSS1):c.40+13C>T rs368872847 0.00016
NM_002769.5(PRSS1):c.508A>G (p.Lys170Glu) rs201550522 0.00006
NM_002769.4(PRSS1):c.-30_-28delTCC rs386134264
NM_002769.5(PRSS1):c.146G>T (p.Gly49Val) rs138464021
NM_002769.5(PRSS1):c.161A>G (p.Asn54Ser) rs144422014
NM_002769.5(PRSS1):c.166C>T (p.Gln56Ter) rs147366981
NM_002769.5(PRSS1):c.200+17C>T rs200688125
NM_002769.5(PRSS1):c.200+17del
NM_002769.5(PRSS1):c.200+1G>A rs143909348
NM_002769.5(PRSS1):c.202C>T (p.Arg68Cys) rs145867820
NM_002769.5(PRSS1):c.255G>A (p.Glu85=) rs376671702
NM_002769.5(PRSS1):c.40C>G (p.Leu14Val) rs747228052
NM_002769.5(PRSS1):c.41-49C>T
NM_002769.5(PRSS1):c.454+16A>T rs377570765
NM_002769.5(PRSS1):c.468C>T (p.Asp156=) rs146076691
NM_002769.5(PRSS1):c.486T>C (p.Asp162=) rs6666
NM_002769.5(PRSS1):c.49C>T (p.Pro17Ser) rs770782578
NM_002769.5(PRSS1):c.542G>A (p.Ser181Asn) rs201719096
NM_002769.5(PRSS1):c.585A>C (p.Ser195=) rs758274784
NM_002769.5(PRSS1):c.588T>C (p.Cys196=) rs751264273
NM_002769.5(PRSS1):c.592-3dup
NM_002769.5(PRSS1):c.617G>C (p.Cys206Ser) rs150930992
NM_002769.5(PRSS1):c.625C>G (p.Gln209Glu)
NM_002769.5(PRSS1):c.637G>A (p.Val213Ile) rs200902389
NM_002769.5(PRSS1):c.651T>C (p.Gly217=) rs562372415
NM_002769.5(PRSS1):c.72C>T (p.Ile24=) rs372637371

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