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

  • See Evidence submitted by expert panel for details.

CA16020842

619160 (ClinVar)

Gene: PAH
Condition: phenylketonuria
Inheritance Mode: Autosomal recessive inheritance
UUID: 2d2e4a9f-fe71-4d44-a8d9-cc64cd71145d
Approved on: 2018-12-10
Published on: 2019-04-05

HGVS expressions

NM_000277.1:c.694C>G
NC_000012.12:g.102855148G>C
CM000674.2:g.102855148G>C
NC_000012.11:g.103248926G>C
CM000674.1:g.103248926G>C
NC_000012.10:g.101773056G>C
NG_008690.1:g.67455C>G
NG_008690.2:g.108263C>G
NM_000277.2:c.694C>G
NM_001354304.1:c.694C>G
NM_000277.3:c.694C>G
ENST00000307000.7:c.679C>G
ENST00000549111.5:n.790C>G
ENST00000553106.5:c.694C>G
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Likely Pathogenic

Met criteria codes 2
PM2 PS3
Not Met criteria codes 1
PP3

Evidence Links 1

Expert Panel

Criteria Specification Information

Criteria Specifications for this VCEP
Evidence submitted by expert panel
Phenylketonuria VCEP
The c.694C>G (p.Gln232Glu) variant in PAH has not been reported in the literature in individuals with PKU. It has been co-expressed with p.E178G and showed 55.0% enzyme activity. PMID: 26803807. BioPKU reports a 42% enzyme activity for this variant (PS3; PMID: 12501224). This variant is absent in population databases (PM2). Computational evidence is conflicting. In summary, this variant meets criteria to be classified as likely pathogenic for PAH. PAH-specific ACMG/AMP criteria applied: PS3, PM2.
Met criteria codes
PM2
Absent from ExAC, gnomAD, 1000G, ESP
PS3
BioPKU: 42% enzyme activity. The co-expression of p.[E178G];[Q232E] showed 55.0% enzyme activity. PMID: 26803807

Not Met criteria codes
PP3
Conflicting predictions
Curation History
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