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TGCAGGAATGCAGCACCACCTTAAA[A/G]AGGAGGGGCAGCTGCTCCAGGGGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602778 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR6A1 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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NR6A1 - nuclear receptor subfamily 6 group A member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278546.1 | 1571 | Silent Mutation | CTC,CTT | L,L 461 | NP_001265475.1 | |
NM_001489.4 | 1571 | Silent Mutation | CTC,CTT | L,L 460 | NP_001480.3 | |
NM_033334.3 | 1571 | Silent Mutation | CTC,CTT | L,L 465 | NP_201591.2 | |
XM_005251917.4 | 1571 | Silent Mutation | CTC,CTT | L,L 464 | XP_005251974.1 | |
XM_005251918.4 | 1571 | Silent Mutation | CTC,CTT | L,L 423 | XP_005251975.1 |