ClinVar Miner

List of variants studied for Phenylketonuria by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_000277.3(PAH):c.1222C>T (p.Arg408Trp) rs5030858 0.00092
NM_000277.3(PAH):c.1208C>T (p.Ala403Val) rs5030857 0.00056
NM_000277.3(PAH):c.1066-11G>A rs5030855 0.00031
NM_000277.3(PAH):c.1241A>G (p.Tyr414Cys) rs5030860 0.00026
NM_000277.3(PAH):c.842C>T (p.Pro281Leu) rs5030851 0.00010
NM_000277.3(PAH):c.1169A>G (p.Glu390Gly) rs5030856 0.00008
NM_000277.3(PAH):c.776C>G (p.Ala259Gly) rs118203921
NM_000277.3(PAH):c.929C>T (p.Ser310Phe) rs62642913

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