ClinVar Miner

List of variants in gene JMJD1C reported as likely benign for not provided

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_032776.3(JMJD1C):c.6570+3G>A rs76935733 0.00908
NM_032776.3(JMJD1C):c.7591G>A (p.Glu2531Lys) rs71508957 0.00482
NM_032776.3(JMJD1C):c.1392G>A (p.Ser464=) rs142118527 0.00326
NM_032776.3(JMJD1C):c.4209C>T (p.Ala1403=) rs193233064 0.00040
NM_032776.3(JMJD1C):c.3807A>G (p.Glu1269=) rs527526754 0.00036
NM_032776.3(JMJD1C):c.4380T>C (p.Ser1460=) rs142996119 0.00019
NM_032776.3(JMJD1C):c.2862T>C (p.His954=) rs370649422 0.00011
NM_032776.3(JMJD1C):c.4069C>T (p.Pro1357Ser) rs200927709 0.00006
NM_032776.3(JMJD1C):c.2637T>G (p.Pro879=) rs759143169 0.00004
NM_032776.3(JMJD1C):c.6912A>G (p.Pro2304=) rs369060332 0.00004
NM_032776.3(JMJD1C):c.7114T>C (p.Leu2372=) rs763845402 0.00004
NM_032776.3(JMJD1C):c.5829T>C (p.Val1943=) rs1467693006 0.00003
NM_032776.3(JMJD1C):c.5350A>G (p.Met1784Val) rs796695209 0.00002
NM_032776.3(JMJD1C):c.1345C>T (p.Arg449Trp) rs778857216 0.00001
NM_032776.3(JMJD1C):c.1920A>G (p.Pro640=) rs1589167008 0.00001
NM_032776.3(JMJD1C):c.2508G>A (p.Leu836=) rs1412063696 0.00001
NM_032776.3(JMJD1C):c.3027G>A (p.Gln1009=) rs1191109718 0.00001
GRCh37/hg19 10q21.3(chr10:65143561-65193646)x1
NM_032776.3(JMJD1C):c.105A>C (p.Arg35=)
NM_032776.3(JMJD1C):c.18G>C (p.Arg6=) rs200305143
NM_032776.3(JMJD1C):c.2475C>T (p.His825=)
NM_032776.3(JMJD1C):c.561T>C (p.Tyr187=) rs769760871
NM_032776.3(JMJD1C):c.5766T>A (p.Thr1922=) rs747909955

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