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_000277.2(PAH):c.745C>T (p.Leu249Phe)

Curation Version - 1.0
Curation History
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CA273356

102821 (ClinVar)

Gene: PAH

Condition: phenylketonuria

Inheritance Mode: Autosomal recessive inheritance

Link to MONDO

UUID: 6807a54c-cde9-445c-b30f-9d4a3fbbdc85

Approved on: 2018-08-12

Published on: 2019-04-05

HGVS expressions

NM_000277.2:c.745C>T

NM_000277.2(PAH):c.745C>T (p.Leu249Phe)

NC_000012.12:g.102852912G>A

CM000674.2:g.102852912G>A

NC_000012.11:g.103246690G>A

CM000674.1:g.103246690G>A

NC_000012.10:g.101770820G>A

NG_008690.1:g.69691C>T

NG_008690.2:g.110499C>T

NM_000277.1:c.745C>T

NM_001354304.1:c.745C>T

NM_000277.3:c.745C>T

ENST00000307000.7:c.730C>T

ENST00000549247.6:n.504C>T

ENST00000553106.5:c.745C>T

Pathogenic

PP4_Moderate PM2 PM3_Very Strong PP3

PS3 PM5

Evidence Links 3

Expert Panel

Phenylketonuria VCEP

Criteria Specification Information

Criteria Specifications for this VCEP

Evidence submitted by expert panel

Phenylketonuria VCEP

PAH-specific ACMG/AMP criteria applied: PM2: Absent from 1000G, ESP. Extremely low frequency in ExAC and gnomAD (0.00004065); PP3: Deleterious effect predicted in SIFT, Polyphen2, MutationTaster. REVEL=0.981; PP4_Moderate: L249F was seen 3 times in HPA patients associated with 2 different haplotypes. DHPR defeciency was excluded. Upgraded per ClinGen Metabolic workgroup. (PMID:8533759); PM3_VeryStrong: Seen with R261X, A309V, V388M, R261Q. All Pathogenic/Likely Pathogenic in ClinVar. Upgraded per ClinGen SVI Workgroup (PMID:21871829; PMID:24765287). In summary this variant meets criteria to be classified as pathogenic for phenylketonuria in an autosomal recessive manner based on the ACMG/AMP criteria applied as specified by the PAH Expert Panel: (PM2, PP3, PP4_Moderate, PM3_VeryStrong).

PP4_Moderate

L249F was seen 3 times in HPA patients associated with 2 different haplotypes. DHPR defeciency was excluded. Upgraded per ClinGen Metabolic workgroup.

A total of 121 Northern Irish families with HPA (111 with PKU and10 with MHP) were investigated, including virtually all patients born after 1972. Dihydrobiopterinreductase deficiency was excluded. L249F was seen 3 times, with 2 different haplotypes (at least 2 different families). PubMed:8533759

PM2

Absent from 1000G, ESP. Extremely low frequency in ExAC and gnomAD (0.00004065)

PM3_Very Strong

Seen with R261X, A309V, V388M, R261Q. All Pathogenic/Likely Pathogenic in ClinVar. Upgraded per ClinGen SVI Workgroup

The diagnosis was confirmed through molecular analysis of the patient as well as the parents. Genetic analysis showed that she is compound heterozygous for the following mutations: p.L249F and p.R261Q (VarID 582, P/LP). The father carries the first mutation and the mother the second. PubMed:24765287

L249F found with p.R261X (Pathogenic) in Patient 47. p.A309V (Path/LP) in Patient 48, p.V388M (Pathogenic) in Patient 49. PubMed:21871829

PP3

Deleterious effect predicted in SIFT, Polyphen2, MutationTaster. REVEL=0.981

PS3

51% enzyme activity in BioPKU

PM5

L249H, no assertion provided

Curation History

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