ClinVar Miner

List of variants in gene CTRC reported as benign for Hereditary pancreatitis

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_007272.3(CTRC):c.640-35G>T rs10927786 0.34421
NM_007272.3(CTRC):c.493+51C>A rs10803384 0.21273
NM_007272.3(CTRC):c.493+52G>A rs545634 0.10881
NM_007272.3(CTRC):c.493+49G>C rs6679763 0.04268
NM_007272.3(CTRC):c.*86A>G rs760937 0.02983
NM_007272.3(CTRC):c.514A>G (p.Lys172Glu) rs34949635 0.02786
NM_007272.3(CTRC):c.*83T>C rs75456156 0.02717
NM_007272.3(CTRC):c.285C>T (p.Asp95=) rs41307798 0.02352
NM_007272.3(CTRC):c.230+38C>T rs115742618 0.01455
NM_007272.3(CTRC):c.156C>T (p.Asn52=) rs77373944 0.00830
NM_007272.3(CTRC):c.690G>A (p.Glu230=) rs75971387 0.00820
NM_007272.3(CTRC):c.760C>T (p.Arg254Trp) rs121909293 0.00386
NM_007272.3(CTRC):c.793-42G>A rs201856611 0.00267
NM_007272.3(CTRC):c.793-45G>T rs199740500 0.00267
NM_007272.3(CTRC):c.640-12G>A rs183053579 0.00194
NM_007272.3(CTRC):c.555G>A (p.Thr185=) rs113087202 0.00097
NM_007272.3(CTRC):c.494-6C>T rs111790169 0.00096
NM_007272.3(CTRC):c.357-44C>G rs200242846 0.00093
NM_007272.3(CTRC):c.640-14C>T rs202049497 0.00060
NM_007272.3(CTRC):c.231-14C>T rs374364850 0.00046
NM_007272.3(CTRC):c.110G>A (p.Arg37Gln) rs145868278 0.00032
NM_007272.3(CTRC):c.703G>A (p.Val235Ile) rs140993290 0.00024
NM_007272.3(CTRC):c.674A>C (p.Glu225Ala) rs201486613 0.00020
NM_007272.3(CTRC):c.747G>A (p.Pro249=) rs150078209 0.00012
NM_007272.3(CTRC):c.533A>G (p.Gln178Arg) rs200678111 0.00009
NM_007272.3(CTRC):c.356+7G>C rs773334021 0.00003
NM_007272.3(CTRC):c.494-13A>G rs762842599 0.00002
NM_007272.3(CTRC):c.369C>T (p.Ala123=) rs749606141 0.00001
NM_007272.3(CTRC):c.68C>T (p.Pro23Leu) rs533967597 0.00001
NM_007272.3(CTRC):c.-59C>T rs183658182
NM_007272.3(CTRC):c.180C>A (p.Gly60=) rs497078
NM_007272.3(CTRC):c.180C>T (p.Gly60=) rs497078
NM_007272.3(CTRC):c.640-34del rs373970317

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