Product Details

SNP ID

rs2186753

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:119045883 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTCAGAAGGGAGGAAGAGGCTAA[C/G]GGAAGGCTGGGCCAGTTTTTCCATG

Phenotype

MIM: 601746

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HYOU1 PubMed Links

Gene Details

Gene

HYOU1

Gene Name

hypoxia up-regulated 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130991.2		Intron			NP_001124463.1
NM_006389.4		Intron			NP_006380.1
XM_005271392.3		Intron			XP_005271449.1
XM_005271393.3		Intron			XP_005271450.1
XM_005271394.3		Intron			XP_005271451.1
XM_017017095.1		Intron			XP_016872584.1
XM_017017096.1		Intron			XP_016872585.1
XM_017017097.1		Intron			XP_016872586.1

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