List of variants in gene ASPM reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.7480T>C (p.Tyr2494His)	rs964201	0.99668
NM_018136.5(ASPM):c.7566A>G (p.Leu2522=)	rs1412640	0.80210
NM_018136.5(ASPM):c.10331+8A>G	rs10754213	0.77181
NM_018136.5(ASPM):c.3579T>A (p.Ser1193=)	rs4915337	0.77164
NM_018136.5(ASPM):c.441+14C>T	rs1571964	0.74895
NM_018136.5(ASPM):c.849C>T (p.Ser283=)	rs6677082	0.74886
NM_018136.5(ASPM):c.7939C>A (p.Leu2647Ile)	rs3762271	0.30411
NM_018136.5(ASPM):c.4449A>G (p.Lys1483=)	rs2878749	0.30404
NM_018136.5(ASPM):c.7684A>G (p.Ser2562Gly)	rs41310927	0.30288
NM_018136.5(ASPM):c.5961A>G (p.Gln1987=)	rs41310925	0.30222
NM_018136.5(ASPM):c.3138G>A (p.Arg1046=)	rs6676084	0.25582
NM_018136.5(ASPM):c.2174-20T>C	rs4915344	0.16253
NM_018136.5(ASPM):c.7605G>A (p.Val2535=)	rs10922162	0.16179
NM_018136.5(ASPM):c.7860G>C (p.Gln2620His)	rs12138336	0.04915
NM_018136.5(ASPM):c.2751C>T (p.Ala917=)	rs33987824	0.01382
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.3742-10T>G	rs41299587	0.00665
NM_018136.5(ASPM):c.5741A>G (p.Gln1914Arg)	rs113325473	0.00427
NM_018136.5(ASPM):c.4213C>T (p.Arg1405Cys)	rs139367209	0.00396
NM_018136.5(ASPM):c.6775T>C (p.Leu2259=)	rs140922974	0.00333
NM_018136.5(ASPM):c.646G>A (p.Glu216Lys)	rs151050191	0.00137
NM_018136.5(ASPM):c.1007C>A (p.Thr336Lys)	rs112113370	0.00066
NM_018136.5(ASPM):c.844A>C (p.Asn282His)	rs113777932	0.00066
NM_018136.5(ASPM):c.905G>A (p.Cys302Tyr)	rs77736715	0.00066
NM_018136.5(ASPM):c.8166T>C (p.Tyr2722=)	rs78315399	0.00046
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.9890C>A (p.Ser3297Tyr)	rs201033114	0.00033
NM_018136.5(ASPM):c.2267A>G (p.Tyr756Cys)	rs201066146	0.00031
NM_018136.5(ASPM):c.937A>G (p.Ile313Val)	rs12025066	0.00029
NM_018136.5(ASPM):c.7114A>G (p.Arg2372Gly)	rs190693455	0.00021
NM_018136.5(ASPM):c.8452G>T (p.Ala2818Ser)	rs188955444	0.00021
NM_018136.5(ASPM):c.8203T>G (p.Phe2735Val)	rs372416792	0.00002
NM_018136.5(ASPM):c.7674C>T (p.Ile2558=)	rs41308365
NM_018136.5(ASPM):c.9395T>G (p.Leu3132Arg)	rs36004306

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