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ACAAGGCTAAAAGAGAGTCAGTGAA[C/T]TGTCCATGGTTTAAGAACTAGGAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 189907 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNF1B 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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HNF1B - HNF1 homeobox B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000458.3 | Intron | NP_000449.1 | ||||
NM_001165923.3 | Intron | NP_001159395.1 | ||||
NM_001304286.1 | Intron | NP_001291215.1 | ||||
XM_011525160.1 | Intron | XP_011523462.1 | ||||
XM_011525161.1 | Intron | XP_011523463.1 | ||||
XM_011525162.2 | Intron | XP_011523464.1 | ||||
XM_011525163.2 | Intron | XP_011523465.1 | ||||
XM_011525164.1 | Intron | XP_011523466.1 |