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CGGTGTCCTCATCTGTTCAATGGGA[C/T]GTTATCAACTTCCTTCTGGGTGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609976 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HIF3A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
HIF3A - hypoxia inducible factor 3 alpha subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022462.4 | Intron | NP_071907.4 | ||||
NM_152794.3 | Intron | NP_690007.1 | ||||
NM_152795.3 | Intron | NP_690008.2 | ||||
NM_152796.2 | Intron | NP_690009.1 | ||||
XM_005259152.4 | Intron | XP_005259209.1 | ||||
XM_005259153.3 | Intron | XP_005259210.2 | ||||
XM_005259155.4 | Intron | XP_005259212.1 | ||||
XM_005259156.4 | Intron | XP_005259213.1 | ||||
XM_017027132.1 | Intron | XP_016882621.1 | ||||
XM_017027133.1 | Intron | XP_016882622.1 | ||||
XM_017027134.1 | Intron | XP_016882623.1 | ||||
XM_017027135.1 | Intron | XP_016882624.1 | ||||
XM_017027136.1 | Intron | XP_016882625.1 | ||||
XM_017027137.1 | Intron | XP_016882626.1 | ||||
XM_017027138.1 | Intron | XP_016882627.1 | ||||
XM_017027139.1 | Intron | XP_016882628.1 | ||||
XM_017027140.1 | Intron | XP_016882629.1 | ||||
XM_017027141.1 | Intron | XP_016882630.1 | ||||
XM_017027142.1 | Intron | XP_016882631.1 |