Product Details

SNP ID

rs1769601

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:33925261 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGTCATTATTTTCAGCAAAATGG[A/G]GCTGAGGCAGAAAATCCAGGTTGCA

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	1142	UTR 3			NP_001295032.1
NM_022073.3	1142	UTR 3			NP_071356.1

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