ClinVar Miner

List of variants in gene TRIP11 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_004239.4(TRIP11):c.5137G>C (p.Glu1713Gln) rs137974620 0.00232
NM_004239.4(TRIP11):c.2102A>G (p.Asn701Ser) rs139539448 0.00217
NM_004239.4(TRIP11):c.5629C>A (p.Pro1877Thr) rs148261539 0.00204
NM_004239.4(TRIP11):c.382G>T (p.Ala128Ser) rs141553918 0.00133
NM_004239.4(TRIP11):c.1280T>C (p.Leu427Ser) rs34761938 0.00103
NM_004239.4(TRIP11):c.4063T>A (p.Ser1355Thr) rs138661581 0.00095
NM_004239.4(TRIP11):c.1952T>C (p.Val651Ala) rs35991093 0.00068
NM_004239.4(TRIP11):c.4173C>T (p.Thr1391=) rs140070005 0.00058
NM_004239.4(TRIP11):c.5537C>T (p.Thr1846Ile) rs141259390 0.00050
NM_004239.4(TRIP11):c.4620T>C (p.Val1540=) rs72705400 0.00049
NM_004239.4(TRIP11):c.5085C>T (p.Leu1695=) rs138379032 0.00035
NM_004239.4(TRIP11):c.1774C>T (p.Leu592=) rs199768095 0.00026
NM_004239.4(TRIP11):c.950A>T (p.Asp317Val) rs140416653 0.00023
NM_004239.4(TRIP11):c.4405G>A (p.Val1469Met) rs147588757 0.00011
NM_004239.4(TRIP11):c.5335G>T (p.Val1779Leu) rs144475398 0.00005
NM_004239.4(TRIP11):c.5574+19C>A rs561150244 0.00003
NM_004239.4(TRIP11):c.4712G>A (p.Arg1571His) rs534500568 0.00001
NM_004239.4(TRIP11):c.499A>G (p.Ile167Val) rs755467642 0.00001
NM_004239.4(TRIP11):c.5051A>G (p.Gln1684Arg) rs764357203 0.00001
NM_004239.4(TRIP11):c.5937A>G (p.Gln1979=) rs762368847 0.00001
NM_004239.4(TRIP11):c.1159G>T (p.Val387Leu) rs376669587
NM_004239.4(TRIP11):c.1191C>G (p.Ala397=) rs886044239
NM_004239.4(TRIP11):c.2584A>C (p.Asn862His) rs886043795
NM_004239.4(TRIP11):c.4691A>C (p.Gln1564Pro) rs886044293
NM_004239.4(TRIP11):c.4892+10del rs794727098
NM_004239.4(TRIP11):c.5829C>T (p.Pro1943=) rs748903681
NM_004239.4(TRIP11):c.660A>G (p.Glu220=) rs1566866887

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