Product Details

SNP ID

rs148617877

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6431282 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGCCTTGGCTGCATTCAGTTTCT[C/G]CACATCACTGTAGCAGTACAAATTG

Phenotype

MIM: 142290

Polymorphism

C/G, Transversion 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	1379	Missense Mutation	CAG,GAG	Q440E	NP_000604.1

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