Product Details

SNP ID

rs1435166

Assay Type

Validated

NCBI dbSNP Submissions

47

Location

Chr.1:231366564 on Build GRCh38

Set Membership

HapMap JSNP Validated

Context Sequence [VIC/FAM]

GCATTCCACTGAATTCCTAAGAGTA[T/C]GGACAATATTTCAACTTTGCAAACA

Phenotype

MIM: 606425

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

EGLN1 PubMed Links

Gene Details

Gene

EGLN1

Gene Name

egl-9 family hypoxia inducible factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022051.2		Intron			NP_071334.1
XM_005273166.4		Intron			XP_005273223.1
XM_005273167.4		Intron			XP_005273224.1

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