ClinVar Miner

List of variants in gene combination PRSS1, TRB reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_002769.5(PRSS1):c.*8A>G rs750733084 0.00010
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.541A>G (p.Ser181Gly) rs376907511 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.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.*12T>C rs749470007 0.00001
NM_002769.5(PRSS1):c.*7C>T rs1334301756 0.00001
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.454+7G>A rs755175379 0.00001
NM_002769.5(PRSS1):c.497T>C (p.Leu166Pro) rs776120935 0.00001
NM_002769.5(PRSS1):c.589C>T (p.Gln197Ter) rs757054367 0.00001
NM_002769.4(PRSS1):c.-28_-8del21 rs755789680
NM_002769.5(PRSS1):c.-10C>A
NM_002769.5(PRSS1):c.1A>G (p.Met1Val)
NM_002769.5(PRSS1):c.1A>T (p.Met1Leu)
NM_002769.5(PRSS1):c.313A>G (p.Asn105Asp)
NM_002769.5(PRSS1):c.325A>C (p.Met109Leu)
NM_002769.5(PRSS1):c.347G>A (p.Arg116His) rs199769221
NM_002769.5(PRSS1):c.386C>T (p.Pro129Leu) rs768673799
NM_002769.5(PRSS1):c.40+15C>T rs760370254
NM_002769.5(PRSS1):c.454+3G>T rs375996400
NM_002769.5(PRSS1):c.468C>G (p.Asp156Glu)
NM_002769.5(PRSS1):c.469G>C (p.Glu157Gln) rs200890507
NM_002769.5(PRSS1):c.50C>A (p.Pro17His)
NM_002769.5(PRSS1):c.50C>T (p.Pro17Leu) rs776401461
NM_002769.5(PRSS1):c.592-4C>G rs375342697
NM_002769.5(PRSS1):c.614T>C (p.Val205Ala) rs747422004
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)

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