Product Details

SNP ID

rs200397325

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6431375 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTTAGGGCCAAGGGACTTTTCCA[C/T]ACACAAGGCTCCGTCTACCTTCTCA

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	1286	Missense Mutation	ATG,GTG	M409V	NP_000604.1

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