ClinVar Miner

List of variants in gene CDH15 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_004933.3(CDH15):c.2025G>A (p.Pro675=) rs62068507 0.00683
NM_004933.3(CDH15):c.387A>G (p.Gly129=) rs147301479 0.00293
NM_004933.3(CDH15):c.160G>A (p.Val54Ile) rs138572161 0.00052
NM_004933.3(CDH15):c.1454C>T (p.Pro485Leu) rs533094369 0.00026
NM_004933.3(CDH15):c.737C>T (p.Ala246Val) rs150599325 0.00026
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.132G>T (p.Arg44=) rs141170431 0.00006
NM_004933.3(CDH15):c.568C>T (p.Arg190Trp) rs137923863 0.00006
NM_004933.3(CDH15):c.2319C>T (p.Phe773=) rs768569547 0.00005
NM_004933.3(CDH15):c.1089C>T (p.Arg363=)
NM_004933.3(CDH15):c.1236C>T (p.Tyr412=)
NM_004933.3(CDH15):c.1305C>G (p.His435Gln)
NM_004933.3(CDH15):c.1383G>A (p.Gln461=)
NM_004933.3(CDH15):c.1453CCG[5] (p.Pro488_Gly489insPro)
NM_004933.3(CDH15):c.1464G>C (p.Pro488=)
NM_004933.3(CDH15):c.1908C>A (p.Gly636=)
NM_004933.3(CDH15):c.1920G>A (p.Leu640=) rs1915708263
NM_004933.3(CDH15):c.1923C>T (p.His641=)
NM_004933.3(CDH15):c.1977C>G (p.Gly659=)
NM_004933.3(CDH15):c.2226C>T (p.Asp742=)
NM_004933.3(CDH15):c.2247G>A (p.Leu749=)
NM_004933.3(CDH15):c.279C>G (p.Gly93=)
NM_004933.3(CDH15):c.291C>T (p.Ile97=)
NM_004933.3(CDH15):c.324C>G (p.Ala108=)
NM_004933.3(CDH15):c.423A>G (p.Val141=) rs772387325
NM_004933.3(CDH15):c.714C>T (p.Asp238=) rs148718049
NM_004933.3(CDH15):c.76A>C (p.Arg26=)
NM_004933.3(CDH15):c.823G>A (p.Gly275Arg)
NM_004933.3(CDH15):c.828G>C (p.Val276=)
NM_004933.3(CDH15):c.890G>A (p.Arg297Lys)
NM_004933.3(CDH15):c.935G>T (p.Arg312Leu)
NM_004933.3(CDH15):c.938C>T (p.Thr313Met)

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