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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