Product Details

SNP ID

hCV30916870

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.1:231370732 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGCCAAATATGTAAGCAGGAGTA[A/C]CCAAAAATGCTACAAGATTAAATTT

Phenotype

MIM: 606425

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

EGLN1 PubMed Links

Gene Details

Gene

EGLN1

Gene Name

egl-9 family hypoxia inducible factor 1

There are no transcripts associated with this gene.

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