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GCAATGACTACATTGTCCCTCGGCA[C/T]TGCCCGGAGCTGGCGGAGATGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600281 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNF4A 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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HNF4A - hepatocyte nuclear factor 4 alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000457.4 | 922 | Silent Mutation | CAC,CAT | H,H 254 | NP_000448.3 | |
NM_001030003.2 | 922 | Silent Mutation | CAC,CAT | H,H 232 | NP_001025174.1 | |
NM_001030004.2 | 922 | Silent Mutation | CAC,CAT | H,H 232 | NP_001025175.1 | |
NM_001258355.1 | 922 | Silent Mutation | CAC,CAT | H,H 247 | NP_001245284.1 | |
NM_001287182.1 | 922 | Silent Mutation | CAC,CAT | H,H 229 | NP_001274111.1 | |
NM_001287183.1 | 922 | Silent Mutation | CAC,CAT | H,H 229 | NP_001274112.1 | |
NM_001287184.1 | 922 | Silent Mutation | CAC,CAT | H,H 229 | NP_001274113.1 | |
NM_175914.4 | 922 | Silent Mutation | CAC,CAT | H,H 232 | NP_787110.2 | |
NM_178849.2 | 922 | Silent Mutation | CAC,CAT | H,H 254 | NP_849180.1 | |
NM_178850.2 | 922 | Silent Mutation | CAC,CAT | H,H 254 | NP_849181.1 | |
XM_005260407.3 | 922 | Silent Mutation | CAC,CAT | H,H 293 | XP_005260464.1 |