ClinVar Miner

List of variants in gene combination CDCA7L, DNAH11 reported by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_018719.5(CDCA7L):c.*980T>C rs7971 0.27747
NM_018719.5(CDCA7L):c.*501T>C rs12700325 0.20592
NM_001277115.2(DNAH11):c.13502A>G (p.Lys4501Arg) rs77448980 0.06056
NM_001277115.2(DNAH11):c.13547C>T (p.Ala4516Val) rs72658840 0.02832
NM_018719.5(CDCA7L):c.*1052G>A rs72658841 0.01754
NM_018719.5(CDCA7L):c.*963G>C rs79947346 0.00244
NM_018719.5(CDCA7L):c.*1006A>G rs573090758 0.00092
NM_001277115.2(DNAH11):c.13548G>A (p.Ala4516=) rs147454485 0.00080
NM_001277115.2(DNAH11):c.13305C>T (p.Gly4435=) rs150682314 0.00029
NM_001277115.2(DNAH11):c.13309C>T (p.Arg4437Cys) rs200466467 0.00027
NM_001277115.2(DNAH11):c.13399G>A (p.Val4467Met) rs200609513 0.00020
NM_018719.5(CDCA7L):c.*805G>A rs192515848 0.00018
NM_018719.5(CDCA7L):c.*912A>G rs547875413 0.00017
NM_001277115.2(DNAH11):c.13398C>T (p.Pro4466=) rs72658836 0.00016
NM_018719.5(CDCA7L):c.*887G>A rs886062191 0.00006
NM_018719.5(CDCA7L):c.*804C>T rs886062192 0.00004
NM_018719.5(CDCA7L):c.*942C>T rs192395057 0.00003
NM_001277115.2(DNAH11):c.13536_13548dup (p.Ter4517AlaextTer?) rs764221599
NM_018719.5(CDCA7L):c.*551CACTGGA[1] rs113860457
NM_018719.5(CDCA7L):c.*766_*769dup rs745609865
NM_018719.5(CDCA7L):c.*788T>C rs1289391313
NM_018719.5(CDCA7L):c.*875G>A rs72658842
NM_018719.5(CDCA7L):c.*879G>C rs62445901
NM_018719.5(CDCA7L):c.*918_*919dup rs886062190
NM_018719.5(CDCA7L):c.*989G>A rs886062189

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