ClinVar Miner

List of variants in gene TPRN reported as benign for not provided

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NC_000009.12:g.137200984C>A rs66708191 0.28691
NM_001128228.3(TPRN):c.559G>T (p.Ala187Ser) rs9411313 0.27092
NM_001128228.3(TPRN):c.1725+151C>T rs72763294 0.22381
NM_001128228.3(TPRN):c.1725+10G>C rs79139547 0.01732
NM_001128228.3(TPRN):c.1073T>C (p.Leu358Pro) rs60910563 0.01648
NM_001128228.3(TPRN):c.1138G>T (p.Ala380Ser) rs190167940 0.01244
NM_001128228.3(TPRN):c.858C>T (p.Cys286=) rs375619082 0.01068
NM_001128228.3(TPRN):c.891C>G (p.Phe297Leu) rs147404722 0.00686
NM_001128228.3(TPRN):c.1929G>A (p.Val643=) rs115446132 0.00458
NM_001128228.3(TPRN):c.533C>T (p.Ala178Val) rs971592946 0.00433
NM_001128228.3(TPRN):c.609C>T (p.Asn203=) rs546101231 0.00320
NM_001128228.3(TPRN):c.969C>T (p.Leu323=) rs145558759 0.00307
NM_001128228.3(TPRN):c.1748A>G (p.Lys583Arg) rs139459217 0.00247
NM_001128228.3(TPRN):c.1256C>T (p.Pro419Leu) rs149753507 0.00148
NM_001128228.3(TPRN):c.1967-26G>A rs375685083 0.00064
NM_001128228.3(TPRN):c.2073+10G>C rs368771637 0.00031
NM_001128228.3(TPRN):c.1094A>G (p.Gln365Arg) rs780953179 0.00028
NM_001128228.3(TPRN):c.1818GGA[10] (p.Glu621dup) rs376810326
NM_001128228.3(TPRN):c.1818GGA[7] (p.Glu620_Glu621del) rs376810326
NM_001128228.3(TPRN):c.1818GGA[8] (p.Glu621del) rs376810326
NM_001128228.3(TPRN):c.894G>A (p.Glu298=) rs539737661

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