Product Details

SNP ID

rs142077509

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6431342 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGAGGTACAAGCCGGGACCATTGG[C/T]GGAACATGAGTTAGGGCCAAGGGAC

Phenotype

MIM: 142290

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HPX PubMed Links

Gene Details

Gene

HPX

Gene Name

hemopexin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000613.2	1319	Missense Mutation	ACC,GCC	T420A	NP_000604.1

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