Product Details

SNP ID
rs200558043
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:128457311 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCTACCTGTTAGGTGTGGTACTG[A/G]CCCTACTCTCCATCTTCGTTAGAGT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HILPDA PubMed Links

Gene Details

Gene
HILPDA
Gene Name
hypoxia inducible lipid droplet associated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098786.1 191 Missense Mutation ACC,GCC T15A NP_001092256.1
NM_013332.3 191 Missense Mutation ACC,GCC T15A NP_037464.1

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