Product Details

SNP ID
rs116630862
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:6449134 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCTGTGGACCATACAGTGGTTCT[A/G]CAGATGTGTTGATATAGGACAGGAA
Phenotype
MIM: 142290 MIM: 605493
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HPX PubMed Links

Gene Details

Gene
HPX
Gene Name
hemopexin
There are no transcripts associated with this gene.

Gene
TRIM3
Gene Name
tripartite motif containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001248006.1 2305 Missense Mutation GCA,GTA A710V NP_001234935.1
NM_001248007.1 2305 Missense Mutation GCA,GTA A591V NP_001234936.1
NM_006458.3 2305 Missense Mutation GCA,GTA A710V NP_006449.2
NM_033278.3 2305 Missense Mutation GCA,GTA A710V NP_150594.2
XM_011519844.1 2305 Missense Mutation GCA,GTA A710V XP_011518146.1
XM_011519845.2 2305 Missense Mutation GCA,GTA A591V XP_011518147.1
XM_017017098.1 2305 Missense Mutation GCA,GTA A710V XP_016872587.1
XM_017017099.1 2305 Missense Mutation GCA,GTA A591V XP_016872588.1

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