List of variants in gene AIPL1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014336.5(AIPL1):c.937G>T (p.Ala313Ser)	rs115681466	0.00535
NM_014336.5(AIPL1):c.140C>G (p.Thr47Arg)	rs150656720	0.00357
NM_014336.5(AIPL1):c.780C>T (p.His260=)	rs145304845	0.00072
NM_014336.5(AIPL1):c.737A>C (p.Tyr246Ser)	rs138585919	0.00021
NM_014336.5(AIPL1):c.562C>T (p.Leu188Phe)	rs146153236	0.00006
NM_014336.5(AIPL1):c.1024C>T (p.Pro342Ser)
NM_014336.5(AIPL1):c.276C>T (p.Ile92=)	rs1064797216

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