Evidence Repository - Clinical Genome Resources

The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]

Variant: NM_000277.1:c.1123C>G

CA6748741

660581 (ClinVar)

Gene: PAH (HGNC:5053)

Condition: phenylketonuria (MONDO:0009861)

Inheritance Mode: Autosomal recessive inheritance

UUID: ba88029d-8764-4060-8a8f-aab28ad4e29b

Approved on: 2020-06-22

Published on: 2021-09-19

HGVS expressions

NM_000277.1:c.1123C>G

NC_000012.12:g.102843722G>C

CM000674.2:g.102843722G>C

NC_000012.11:g.103237500G>C

CM000674.1:g.103237500G>C

NC_000012.10:g.101761630G>C

NG_008690.1:g.78881C>G

NG_008690.2:g.119689C>G

ENST00000553106.6:c.1123C>G

ENST00000307000.7:c.1108C>G

ENST00000549247.6:n.882C>G

ENST00000551114.2:n.785C>G

ENST00000553106.5:c.1123C>G

ENST00000635477.1:n.227C>G

ENST00000635528.1:n.638C>G

NM_000277.2:c.1123C>G

NM_001354304.1:c.1123C>G

NM_000277.3:c.1123C>G

NM_001354304.2:c.1123C>G

Likely Pathogenic

PM3_Very Strong PP4_Moderate

PM5 PM2 PP3

Evidence Links 1

Expert Panel

Phenylketonuria VCEP

Criteria Specification Information

Criteria Specifications for this VCEP

Evidence submitted by expert panel

Phenylketonuria VCEP

The c.1123C>G (p.Gln375Glu) variant in PAH has been reported in multiple individuals with PAH deficiency (BH4 deficiency excluded, PMID:26503515). It was detected in trans with pathogenic variants: p.Arg243Gln; p.Arg408Trp; EX6-96A＞G (PMID: 28982351); c.977G>A (p.W326*); p.R413P (PMID: 3005010). This variant has an allele frequency in gnomAD (MAF=0.0003808) that is above the PAH VCEP cutoff for pathogenicity (0.0002). Computational evidence is conflicting. In summary, this variant meets criteria to be classified as likely pathogenic for PAH. PAH-specific ACMG/AMP criteria applied: PP4_Moderate, PM3_very-strong.

PM3_Very Strong

Detected with p.Arg243Gln (P 11 submitters); p.Arg408Trp (P 17 submitters); EX6-96A＞G (P 6 submitters); variable sites in patient genes were aligned with the corresponding sites from the respective parents. PMID: 28982351; c.977G>A (p.W326*) (P 1 submitter); p.R413P (P 6 submitters) The validation tests on parents were performed using Sanger sequencing. PMID: 30050108 5.0 pts

PP4_Moderate

Seen in 2 individuals with Classic PKU. Biochemical testing data, including plasma phenylalanine (Phe) levels, dihydropteridine reductase activity, urinary biopterin and neopterin ratio, and tetrahydrobiopterin loading, were collected. PMID: 26503515

PM5

No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline

PM2

Seen in low frequency: gnomAD (MAF=0.0003808)

PP3

Tolerated by SIFT, deleterious by MutationTaster and PolyPhen.

Curation History

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