Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTTCCTTTTCGTCTCGTAAAGGAG[A/T]GAGAAGTGCAGAGTTCGATTCTGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602408 MIM: 190120 | ||||||||||||||||||||
Literature Links: |
NR1D1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NR1D1 - nuclear receptor subfamily 1 group D member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021724.4 | 1689 | UTR 3 | NP_068370.1 |
THRA - thyroid hormone receptor, alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190918.1 | 1689 | Intron | NP_001177847.1 | |||
NM_001190919.1 | 1689 | Nonsense Mutation | AGA,TGA | R,* 372 | NP_001177848.1 | |
NM_003250.5 | 1689 | Nonsense Mutation | AGA,TGA | R,* 372 | NP_003241.2 | |
NM_199334.3 | 1689 | Intron | NP_955366.1 |