Product Details

SNP ID
rs142517237
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:46303928 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACGGAGCTGCGCAAGGAAAAGTC[C/T]CGGGATGCGGCCCGCAGCCGGCGCA
Phenotype
MIM: 609976
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HIF3A PubMed Links

Gene Details

Gene
HIF3A
Gene Name
hypoxia inducible factor 3 alpha subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022462.4 216 UTR 5 NP_071907.4
NM_152794.3 216 Silent Mutation TCC,TCT S17S NP_690007.1
NM_152795.3 216 Silent Mutation TCC,TCT S19S NP_690008.2
NM_152796.2 216 UTR 5 NP_690009.1
XM_005259152.4 216 Silent Mutation TCC,TCT S63S XP_005259209.1
XM_005259153.3 216 UTR 5 XP_005259210.2
XM_005259155.4 216 Silent Mutation TCC,TCT S63S XP_005259212.1
XM_005259156.4 216 Silent Mutation TCC,TCT S63S XP_005259213.1
XM_017027132.1 216 Silent Mutation TCC,TCT S63S XP_016882621.1
XM_017027133.1 216 Silent Mutation TCC,TCT S63S XP_016882622.1
XM_017027134.1 216 Silent Mutation TCC,TCT S19S XP_016882623.1
XM_017027135.1 216 Silent Mutation TCC,TCT S17S XP_016882624.1
XM_017027136.1 216 Silent Mutation TCC,TCT S63S XP_016882625.1
XM_017027137.1 216 Silent Mutation TCC,TCT S17S XP_016882626.1
XM_017027138.1 216 Silent Mutation TCC,TCT S19S XP_016882627.1
XM_017027139.1 216 UTR 5 XP_016882628.1
XM_017027140.1 216 UTR 5 XP_016882629.1
XM_017027141.1 216 UTR 5 XP_016882630.1
XM_017027142.1 216 UTR 5 XP_016882631.1

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