Product Details

SNP ID
rs113379201
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119046422 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCATGGTTGCTCCAACTCACCAGTC[C/T]CTACTTTCTCAGGTTCTGAAATGGG
Phenotype
MIM: 601746
Polymorphism
C/T, Transition 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 2977 Missense Mutation GAG,GGG E961G NP_001124463.1
NM_006389.4 2977 Missense Mutation GAG,GGG E961G NP_006380.1
XM_005271392.3 2977 Missense Mutation GAG,GGG E961G XP_005271449.1
XM_005271393.3 2977 Missense Mutation GAG,GGG E961G XP_005271450.1
XM_005271394.3 2977 Missense Mutation GAG,GGG E961G XP_005271451.1
XM_017017095.1 2977 Missense Mutation GAG,GGG E961G XP_016872584.1
XM_017017096.1 2977 Missense Mutation GAG,GGG E961G XP_016872585.1
XM_017017097.1 2977 Missense Mutation GAG,GGG E961G XP_016872586.1

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