ClinVar Miner

List of variants in gene PRSS1, TRB studied for not specified

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Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_002769.5(PRSS1):c.738T>C (p.Asn246=) rs6667 0.53816
NM_002769.5(PRSS1):c.40+34C>T rs202051517 0.00687
NM_002769.5(PRSS1):c.200+23C>T rs112426474 0.00622
NM_002769.5(PRSS1):c.567T>C (p.Leu189=) rs377124851 0.00444
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.623G>C (p.Gly208Ala) rs189270875 0.00024
NM_002769.5(PRSS1):c.621T>C (p.Asn207=) rs146995038 0.00020
NM_002769.5(PRSS1):c.453C>T (p.Gly151=) rs147765409 0.00018
NM_002769.5(PRSS1):c.40+13C>T rs368872847 0.00016
NM_002769.5(PRSS1):c.390C>T (p.Thr130=) rs561097415 0.00012
NM_002769.5(PRSS1):c.243G>C (p.Leu81=) rs142476093 0.00011
NM_002769.5(PRSS1):c.235G>A (p.Glu79Lys) rs111033564 0.00010
NM_002769.5(PRSS1):c.283C>T (p.Arg95Cys) rs201775810 0.00010
NM_002769.5(PRSS1):c.284G>A (p.Arg95His) rs375820192 0.00008
NM_002769.5(PRSS1):c.508A>G (p.Lys170Glu) rs201550522 0.00006
NM_002769.5(PRSS1):c.541A>G (p.Ser181Gly) rs376907511 0.00006
NM_002769.5(PRSS1):c.674A>G (p.Lys225Arg) rs541223359 0.00006
NM_002769.5(PRSS1):c.247G>C (p.Gly83Arg) rs372411481 0.00004
NM_002769.5(PRSS1):c.200+10G>T rs200217253 0.00003
NM_002769.5(PRSS1):c.200+18G>A rs778658500 0.00003
NM_002769.5(PRSS1):c.200C>T (p.Ser67Phe) rs765342413 0.00002
NM_002769.5(PRSS1):c.240C>T (p.Val80=) rs772622287 0.00002
NM_002769.5(PRSS1):c.292C>A (p.Gln98Lys) rs750348889 0.00002
NM_002769.5(PRSS1):c.35C>T (p.Ala12Val) rs772363999 0.00002
NM_002769.5(PRSS1):c.361G>A (p.Ala121Thr) rs199422123 0.00002
NM_002769.5(PRSS1):c.454+5G>T rs1468322371 0.00002
NM_002769.5(PRSS1):c.-2C>A rs766465080 0.00001
NM_002769.5(PRSS1):c.163G>C (p.Glu55Gln) rs1365488828 0.00001
NM_002769.5(PRSS1):c.200+8T>C rs886038518 0.00001
NM_002769.5(PRSS1):c.201-37G>T rs774875799 0.00001
NM_002769.5(PRSS1):c.454+7G>A rs755175379 0.00001
NM_002769.5(PRSS1):c.497T>C (p.Leu166Pro) rs776120935 0.00001
NM_002769.5(PRSS1):c.561C>T (p.Gly187=) rs1804561 0.00001
NM_002769.5(PRSS1):c.589C>T (p.Gln197Ter) rs757054367 0.00001
NM_002769.5(PRSS1):c.592-9T>C rs766186870 0.00001
NM_002769.5(PRSS1):c.93G>A (p.Glu31=) rs745623963 0.00001
NM_002769.4(PRSS1):c.-28_-8del21 rs755789680
NM_002769.4(PRSS1):c.-30_-28delTCC rs386134264
NM_002769.5(PRSS1):c.-10C>A
NM_002769.5(PRSS1):c.146G>T (p.Gly49Val) rs138464021
NM_002769.5(PRSS1):c.162C>T (p.Asn54=) rs148440491
NM_002769.5(PRSS1):c.1A>G (p.Met1Val)
NM_002769.5(PRSS1):c.1A>T (p.Met1Leu)
NM_002769.5(PRSS1):c.200+17C>T rs200688125
NM_002769.5(PRSS1):c.200+1G>A rs143909348
NM_002769.5(PRSS1):c.311T>C (p.Leu104Pro) rs1554499091
NM_002769.5(PRSS1):c.313A>G (p.Asn105Asp)
NM_002769.5(PRSS1):c.325A>C (p.Met109Leu)
NM_002769.5(PRSS1):c.328T>C (p.Leu110=)
NM_002769.5(PRSS1):c.330A>G (p.Leu110=)
NM_002769.5(PRSS1):c.347G>A (p.Arg116His) rs199769221
NM_002769.5(PRSS1):c.360C>T (p.Asn120=) rs606231348
NM_002769.5(PRSS1):c.386C>T (p.Pro129Leu) rs768673799
NM_002769.5(PRSS1):c.40+15C>T rs760370254
NM_002769.5(PRSS1):c.40+36C>G rs200529674
NM_002769.5(PRSS1):c.40+40C>T rs200159984
NM_002769.5(PRSS1):c.40+40del rs748794481
NM_002769.5(PRSS1):c.41-45del
NM_002769.5(PRSS1):c.444G>A (p.Ala148=) rs11553844
NM_002769.5(PRSS1):c.454+16A>T rs377570765
NM_002769.5(PRSS1):c.454+3G>T rs375996400
NM_002769.5(PRSS1):c.468C>G (p.Asp156Glu)
NM_002769.5(PRSS1):c.468C>T (p.Asp156=) rs146076691
NM_002769.5(PRSS1):c.469G>C (p.Glu157Gln) rs200890507
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.50C>A (p.Pro17His)
NM_002769.5(PRSS1):c.50C>T (p.Pro17Leu) rs776401461
NM_002769.5(PRSS1):c.510G>A (p.Lys170=) rs750427023
NM_002769.5(PRSS1):c.529G>T (p.Gly177Ter) rs1240508430
NM_002769.5(PRSS1):c.542G>A (p.Ser181Asn) rs201719096
NM_002769.5(PRSS1):c.592-2A>C rs1585991476
NM_002769.5(PRSS1):c.592-4C>G rs375342697
NM_002769.5(PRSS1):c.614T>C (p.Val205Ala) rs747422004
NM_002769.5(PRSS1):c.637G>A (p.Val213Ile) rs200902389
NM_002769.5(PRSS1):c.651_652delinsCT (p.Asp218Tyr) rs1554499629
NM_002769.5(PRSS1):c.659G>A (p.Cys220Tyr)
NM_002769.5(PRSS1):c.694G>T (p.Val232Phe)
NM_002769.5(PRSS1):c.72C>T (p.Ile24=) rs372637371

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