Product Details

SNP ID

rs150488733

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6431465 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTTCAGGTCCAGCCACCACAGCC[A/G]CCGTCCTGGGGAGAAGGCACCAAAC

Phenotype

MIM: 142290

Polymorphism

A/G, 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	1196	Missense Mutation	CGG,TGG	R379W	NP_000604.1

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