ClinVar Miner

List of variants in gene CDHR1 reported as likely benign

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Total variants: 41
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HGVS dbSNP
NM_033100.4(CDHR1):c.*134C>T rs41291356
NM_033100.4(CDHR1):c.*1383dup rs147801078
NM_033100.4(CDHR1):c.*173C>A rs41291358
NM_033100.4(CDHR1):c.*2589G>A rs56127582
NM_033100.4(CDHR1):c.*342C>G rs7908492
NM_033100.4(CDHR1):c.*394G>A rs7907675
NM_033100.4(CDHR1):c.*503C>T rs7908753
NM_033100.4(CDHR1):c.*893C>T rs6585846
NM_033100.4(CDHR1):c.*907G>A rs12356218
NM_033100.4(CDHR1):c.1071C>T (p.Ser357=) rs146588811
NM_033100.4(CDHR1):c.1206C>T (p.Pro402=) rs149181127
NM_033100.4(CDHR1):c.1359T>C (p.Ser453=)
NM_033100.4(CDHR1):c.1431C>T (p.Tyr477=)
NM_033100.4(CDHR1):c.1461G>A (p.Gly487=) rs141787212
NM_033100.4(CDHR1):c.1515C>T (p.Gly505=) rs116594644
NM_033100.4(CDHR1):c.1518A>G (p.Glu506=)
NM_033100.4(CDHR1):c.152-9T>C rs754726772
NM_033100.4(CDHR1):c.1553+6T>C rs199567321
NM_033100.4(CDHR1):c.1770A>G (p.Pro590=)
NM_033100.4(CDHR1):c.1792G>A (p.Glu598Lys)
NM_033100.4(CDHR1):c.183C>T (p.Asp61=)
NM_033100.4(CDHR1):c.1868A>G (p.Asn623Ser) rs137876961
NM_033100.4(CDHR1):c.1873C>G (p.His625Asp) rs149043166
NM_033100.4(CDHR1):c.1906C>T (p.Arg636Cys)
NM_033100.4(CDHR1):c.2055C>T (p.Ser685=) rs141036655
NM_033100.4(CDHR1):c.216C>T (p.Ser72=)
NM_033100.4(CDHR1):c.2352A>G (p.Glu784=)
NM_033100.4(CDHR1):c.2367G>A (p.Pro789=) rs150097621
NM_033100.4(CDHR1):c.240C>T (p.Val80=) rs11593005
NM_033100.4(CDHR1):c.2434C>T (p.Pro812Ser) rs45584033
NM_033100.4(CDHR1):c.2493T>C (p.Thr831=)
NM_033100.4(CDHR1):c.2546_2548AGA[2] (p.Lys851del)
NM_033100.4(CDHR1):c.297+6G>A rs79239487
NM_033100.4(CDHR1):c.408C>T (p.Ile136=) rs148125234
NM_033100.4(CDHR1):c.486G>C (p.Arg162Ser) rs74145715
NM_033100.4(CDHR1):c.526-7C>G rs190906755
NM_033100.4(CDHR1):c.526-8T>C
NM_033100.4(CDHR1):c.728C>T (p.Ala243Val) rs7086200
NM_033100.4(CDHR1):c.75G>T (p.Pro25=)
NM_033100.4(CDHR1):c.863-9C>T rs4933977
NM_033100.4(CDHR1):c.964-10C>T rs886047327

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