ClinVar Miner

List of variants in gene CDH15 reported by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_004933.3(CDH15):c.1971A>G (p.Gln657=) rs3815615 0.42410
NM_004933.3(CDH15):c.264T>C (p.Asp88=) rs59865771 0.29473
NM_004933.3(CDH15):c.1023G>A (p.Ser341=) rs72819366 0.15210
NM_004933.3(CDH15):c.109G>T (p.Ala37Ser) rs2287359 0.06504
NM_004933.3(CDH15):c.174C>T (p.His58=) rs2287358 0.04202
NM_004933.3(CDH15):c.153G>A (p.Pro51=) rs76549400 0.01905
NM_004933.3(CDH15):c.615C>T (p.Asp205=) rs148424541 0.01282
NM_004933.3(CDH15):c.171C>T (p.Asn57=) rs148798647 0.01145
NM_004933.3(CDH15):c.2025G>A (p.Pro675=) rs62068507 0.00683
NM_004933.3(CDH15):c.718C>T (p.Leu240Phe) rs142647750 0.00509
NM_004933.3(CDH15):c.387A>G (p.Gly129=) rs147301479 0.00293
NM_004933.3(CDH15):c.598G>A (p.Glu200Lys) rs141084668 0.00098
NM_004933.3(CDH15):c.2237C>T (p.Ala746Val) rs139450416 0.00051
NM_004933.3(CDH15):c.669C>A (p.Val223=) rs138351924 0.00043
NM_004933.3(CDH15):c.2146A>G (p.Asn716Asp) rs147397532 0.00037
NM_004933.3(CDH15):c.1454C>T (p.Pro485Leu) rs533094369 0.00026
NM_004933.3(CDH15):c.1615+3G>A rs755682005 0.00015
NM_004933.3(CDH15):c.1680G>T (p.Leu560=) rs779984001 0.00015
NM_004933.3(CDH15):c.2369C>T (p.Ala790Val) rs146594802 0.00014
NM_004933.3(CDH15):c.107G>A (p.Arg36Gln) rs367770505 0.00013
NM_004933.3(CDH15):c.1320G>A (p.Ala440=) rs373183010 0.00013
NM_004933.3(CDH15):c.274C>T (p.Arg92Trp) rs121434540 0.00011
NM_004933.3(CDH15):c.2159A>C (p.Glu720Ala) rs370967218 0.00010
NM_004933.3(CDH15):c.2319C>T (p.Phe773=) rs768569547 0.00005
NM_004933.3(CDH15):c.165C>T (p.Ser55=) rs533141968 0.00004
NM_004933.3(CDH15):c.616G>A (p.Glu206Lys) rs779397293 0.00004
NM_004933.3(CDH15):c.227G>A (p.Gly76Asp) rs587780299 0.00003
NM_004933.3(CDH15):c.671C>T (p.Ala224Val) rs587780300 0.00003
NM_004933.3(CDH15):c.280G>A (p.Val94Ile) rs369126978 0.00002
NM_004933.3(CDH15):c.402C>T (p.Asp134=) rs777715571 0.00002
NM_004933.3(CDH15):c.1211C>T (p.Thr404Ile) rs374288437 0.00001
NM_004933.3(CDH15):c.782C>A (p.Thr261Asn) rs587780301 0.00001
NM_004933.3(CDH15):c.788A>G (p.Asp263Gly) rs587780302 0.00001
NM_004933.3(CDH15):c.1162G>A (p.Ala388Thr) rs747009056
NM_004933.3(CDH15):c.1387C>T (p.Arg463Cys) rs779657883
NM_004933.3(CDH15):c.1531C>G (p.Pro511Ala) rs1419856684
NM_004933.3(CDH15):c.1912G>C (p.Gly638Arg) rs138712131
NM_004933.3(CDH15):c.1920G>A (p.Leu640=) rs1915708263
NM_004933.3(CDH15):c.2042C>T (p.Pro681Leu) rs910602813
NM_004933.3(CDH15):c.2051C>T (p.Pro684Leu) rs1457517527
NM_004933.3(CDH15):c.2226C>A (p.Asp742Glu) rs370556933
NM_004933.3(CDH15):c.2353G>A (p.Gly785Arg) rs149307887
NM_004933.3(CDH15):c.2364C>A (p.Tyr788Ter) rs2270416
NM_004933.3(CDH15):c.633C>A (p.Ile211=) rs531999031
NM_004933.3(CDH15):c.938C>G (p.Thr313Arg) rs758656978
NM_004933.3(CDH15):c.970A>G (p.Ile324Val) rs1348481251

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