Product Details

SNP ID
rs148786669
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:6449041 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTCTGTACAGCTACTGGAGGTAG[C/T]GATAGGCTTTAAAGCAGTGGTTGCC
Phenotype
MIM: 142290 MIM: 605493
Polymorphism
C/T, 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 2398 Missense Mutation CAC,CGC H741R NP_001234935.1
NM_001248007.1 2398 Missense Mutation CAC,CGC H622R NP_001234936.1
NM_006458.3 2398 Missense Mutation CAC,CGC H741R NP_006449.2
NM_033278.3 2398 Missense Mutation CAC,CGC H741R NP_150594.2
XM_011519844.1 2398 Missense Mutation CAC,CGC H741R XP_011518146.1
XM_011519845.2 2398 Missense Mutation CAC,CGC H622R XP_011518147.1
XM_017017098.1 2398 Missense Mutation CAC,CGC H741R XP_016872587.1
XM_017017099.1 2398 Missense Mutation CAC,CGC H622R XP_016872588.1

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