List of variants in gene combination FAM20A, PRKAR1A reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.928+16G>A	rs16973042	0.01441
NM_017565.4(FAM20A):c.1314C>T (p.His438=)	rs78050433	0.00053
NM_017565.4(FAM20A):c.1175G>A (p.Arg392Gln)	rs376802484	0.00016
NM_017565.4(FAM20A):c.1472C>T (p.Thr491Ile)	rs182816928	0.00015
NM_017565.4(FAM20A):c.792C>T (p.Ile264=)	rs139591838	0.00014
NM_017565.4(FAM20A):c.984T>C (p.Ala328=)	rs374633547	0.00011
NM_017565.4(FAM20A):c.826C>T (p.Arg276Ter)	rs387907215	0.00001
NM_017565.4(FAM20A):c.1094T>C (p.Leu365Pro)	rs956049429
NM_017565.4(FAM20A):c.1169G>A (p.Ser390Asn)	rs771912912
NM_017565.4(FAM20A):c.1294G>A (p.Ala432Thr)	rs200599944
NM_017565.4(FAM20A):c.757T>C (p.Tyr253His)	rs2143526028
NM_017565.4(FAM20A):c.915_918del (p.Phe305fs)	rs760163489

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