ClinVar Miner

List of variants reported as likely benign for Microcephaly 5, primary, autosomal recessive by Illumina Laboratory Services, Illumina

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_018136.5(ASPM):c.*60C>T rs1537318 0.02044
NM_018136.5(ASPM):c.-110C>T rs74981632 0.01875
NM_018136.5(ASPM):c.2419+12G>A rs77191836 0.01806
NM_018136.5(ASPM):c.2751C>T (p.Ala917=) rs33987824 0.01382
NM_018136.5(ASPM):c.7917A>G (p.Lys2639=) rs112647911 0.00953
NM_018136.5(ASPM):c.7353G>A (p.Leu2451=) rs111487086 0.00949
NM_018136.5(ASPM):c.5185C>T (p.Arg1729Trp) rs41299623 0.00808
NM_018136.5(ASPM):c.9773A>G (p.His3258Arg) rs7528827 0.00754
NM_018136.5(ASPM):c.5629G>A (p.Ala1877Thr) rs112230218 0.00719
NM_018136.5(ASPM):c.3742-10T>G rs41299587 0.00649
NM_018136.5(ASPM):c.1987G>T (p.Ala663Ser) rs113611857 0.00638
NM_018136.5(ASPM):c.3741+3A>G rs138558822 0.00594
NM_018136.5(ASPM):c.6727G>T (p.Val2243Leu) rs148425392 0.00493
NM_018136.5(ASPM):c.-28G>A rs111299108 0.00419
NM_018136.5(ASPM):c.5741A>G (p.Gln1914Arg) rs113325473 0.00402
NM_018136.5(ASPM):c.4213C>T (p.Arg1405Cys) rs139367209 0.00396
NM_018136.5(ASPM):c.7554A>G (p.Arg2518=) rs140248383 0.00361
NM_018136.5(ASPM):c.3791G>A (p.Arg1264His) rs150125249 0.00357
NM_018136.5(ASPM):c.6775T>C (p.Leu2259=) rs140922974 0.00304
NM_018136.5(ASPM):c.9444+8T>G rs140150599 0.00259
NM_018136.5(ASPM):c.9996T>C (p.Thr3332=) rs139927527 0.00253
NM_018136.5(ASPM):c.9539A>C (p.Gln3180Pro) rs193251130 0.00130
NM_018136.5(ASPM):c.-114C>A rs78280885 0.00121
NM_018136.5(ASPM):c.1732G>A (p.Asp578Asn) rs60950503 0.00119
NM_018136.5(ASPM):c.-177G>A rs80055790 0.00118
NM_018136.5(ASPM):c.-9G>T rs141108591 0.00105
NM_018136.5(ASPM):c.1007C>A (p.Thr336Lys) rs112113370 0.00094
NM_018136.5(ASPM):c.844A>C (p.Asn282His) rs113777932 0.00094
NM_018136.5(ASPM):c.8449G>T (p.Ala2817Ser) rs117963393 0.00087
NM_018136.5(ASPM):c.8166T>C (p.Tyr2722=) rs78315399 0.00070
NM_018136.5(ASPM):c.905G>A (p.Cys302Tyr) rs77736715 0.00066
NM_018136.5(ASPM):c.9492T>C (p.Tyr3164=) rs143931757 0.00061
NM_018136.5(ASPM):c.2267A>G (p.Tyr756Cys) rs201066146 0.00049
NM_018136.5(ASPM):c.937A>G (p.Ile313Val) rs12025066 0.00040
NM_018136.5(ASPM):c.581C>A (p.Ala194Asp) rs141532484 0.00038
NM_018136.5(ASPM):c.7475G>A (p.Arg2492Lys) rs118010078 0.00037
NM_018136.5(ASPM):c.5224T>C (p.Tyr1742His) rs143733126 0.00019
NM_018136.5(ASPM):c.8203T>G (p.Phe2735Val) rs372416792 0.00002

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