ClinVar

NM_000277.3(PAH):c.995G>A (p.Gly332Glu)

Gene:

PAH:phenylalanine hydroxylase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q23.2

Genomic location:

• Chr12: 102844406 (on Assembly GRCh38)
• Chr12: 103238184 (on Assembly GRCh37)

Preferred name:

NM_000277.3(PAH):c.995G>A (p.Gly332Glu)

HGVS:

• NC_000012.12:g.102844406C>T
• NG_008690.2:g.119005G>A
• NM_000277.3:c.995G>AMANE SELECT
• NM_001354304.2:c.995G>A
• NP_000268.1:p.Gly332Glu
• NP_001341233.1:p.Gly332Glu
• NC_000012.11:g.103238184C>T
• NM_000277.1:c.995G>A

This HGVS expression did not pass validation

Protein change:

G332E

Links:

dbSNP: rs62508589

NCBI 1000 Genomes Browser:

rs62508589

Molecular consequence:

• NM_000277.3:c.995G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354304.2:c.995G>A - missense variant - [Sequence Ontology: SO:0001583]