Product Details

SNP ID
rs1384375
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:33925193 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGGGGAATTAGGTTCCCAGGTAA[A/G]AACTGAAAATGGAGAAAAAATTGTG
Phenotype
MIM: 606426
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
EGLN3 PubMed Links

Gene Details

Gene
EGLN3
Gene Name
egl-9 family hypoxia inducible factor 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308103.1 1210 UTR 3 NP_001295032.1
NM_022073.3 1210 UTR 3 NP_071356.1

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