ClinVar Miner

List of variants in gene NBPF10 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001302371.3(NBPF10):c.373G>C (p.Glu125Gln) rs140256918 0.00830
NM_001302371.3(NBPF10):c.2004T>A (p.Val668=) rs200583985 0.00704
NM_001302371.3(NBPF10):c.11301C>T (p.Phe3767=) rs782343714 0.00646
NM_001302371.3(NBPF10):c.1377C>T (p.Pro459=) rs201134964 0.00608
NM_001302371.3(NBPF10):c.1314C>G (p.Asp438Glu) rs202002098 0.00422
NM_001302371.3(NBPF10):c.1092-7A>G rs200948811 0.00298
NM_001302371.3(NBPF10):c.1928C>G (p.Pro643Arg) rs587689248 0.00079
NM_001302371.3(NBPF10):c.2057A>T (p.Asp686Val) rs782345277 0.00061
NM_001302371.3(NBPF10):c.30T>C (p.Ser10=) rs60398273 0.00015
NM_001302371.3(NBPF10):c.10782G>A (p.Gln3594=) rs587678061 0.00008
NM_001302371.3(NBPF10):c.1221G>A (p.Pro407=) rs587773151 0.00004
NM_001302371.3(NBPF10):c.1638-8C>T rs201947016 0.00002
NM_001302371.3(NBPF10):c.10170C>A (p.Val3390=)
NM_001302371.3(NBPF10):c.10703A>C (p.Tyr3568Ser) rs587638297
NM_001302371.3(NBPF10):c.10810+8C>G rs781807043
NM_001302371.3(NBPF10):c.10962C>T (p.Asp3654=)
NM_001302371.3(NBPF10):c.11010C>T (p.Tyr3670=)
NM_001302371.3(NBPF10):c.1114G>A (p.Ala372Thr) rs200242621
NM_001302371.3(NBPF10):c.1290C>A (p.Val430=) rs1270965264
NM_001302371.3(NBPF10):c.1475A>G (p.Asn492Ser) rs782302575
NM_001302371.3(NBPF10):c.1771C>A (p.Gln591Lys) rs782751843
NM_001302371.3(NBPF10):c.1962G>A (p.Gln654=) rs782443316
NM_001302371.3(NBPF10):c.346G>T (p.Gly116Trp) rs186121989
NM_001302371.3(NBPF10):c.4104G>A (p.Leu1368=) rs782120834
NM_001302371.3(NBPF10):c.4138G>C (p.Glu1380Gln) rs781922025
NM_001302371.3(NBPF10):c.4459G>A (p.Asp1487Asn) rs587698666
NM_001302371.3(NBPF10):c.4487C>G (p.Pro1496Arg) rs587622326
NM_001302371.3(NBPF10):c.4821C>G (p.Val1607=) rs1553785158
NM_001302371.3(NBPF10):c.4836G>A (p.Leu1612=) rs2526087518
NM_001302371.3(NBPF10):c.4953T>C (p.Asp1651=) rs782089046
NM_001302371.3(NBPF10):c.597C>T (p.Val199=)
NM_001302371.3(NBPF10):c.792C>G (p.Thr264=) rs782099305
NM_001302371.3(NBPF10):c.8271C>G (p.Pro2757=)
NM_001302371.3(NBPF10):c.8322T>C (p.Leu2774=)
NM_001302371.3(NBPF10):c.84G>T (p.Leu28=)
NM_001302371.3(NBPF10):c.9024A>G (p.Ala3008=) rs1270653449
NM_001302371.3(NBPF10):c.9231T>G (p.Asp3077Glu) rs1553781235
NM_001302371.3(NBPF10):c.9262G>T (p.Glu3088Ter) rs587768370
NM_001302371.3(NBPF10):c.9268= (p.Thr3090=)
NM_001302371.3(NBPF10):c.9428= (p.Glu3143=)
NM_001302371.3(NBPF10):c.957C>T (p.Ser319=)

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