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TAAATAGCTATGAAATGAGAAAATA[A/G]TTCTTACTTTCAAAGTACATATGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605966 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNF4G PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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HNF4G - hepatocyte nuclear factor 4 gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004133.4 | Intron | NP_004124.4 | ||||
XM_011517516.2 | Intron | XP_011515818.1 | ||||
XM_017013373.1 | Intron | XP_016868862.1 | ||||
XM_017013374.1 | Intron | XP_016868863.1 | ||||
XM_017013375.1 | Intron | XP_016868864.1 | ||||
XM_017013376.1 | Intron | XP_016868865.1 |