Product Details

SNP ID

rs199475696

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:102840453 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCTGGGTATTGTCCAAGACCTCA[G/A]TCCTTTGGGTGTATGGGTCGTAGCG

Phenotype

MIM: 612349

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

PAH PubMed Links

Gene Details

Gene

PAH

Gene Name

phenylalanine hydroxylase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000277.1	1734	Missense Mutation	ACT,ATT	T421I	NP_000268.1
XM_017019370.1	1734	Intron			XP_016874859.1

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