Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGAAAGTCACGTGGTCTTTGAGAC[A/C]ATTTACAATCTTGTTTTGCAGTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601828 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR4A2 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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NR4A2 - nuclear receptor subfamily 4 group A member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006186.3 | 3731 | Missense Mutation | GGT,TGT | G,C 534 | NP_006177.1 | |
XM_005246621.3 | 3731 | Missense Mutation | GGT,TGT | G,C 545 | XP_005246678.1 | |
XM_005246622.3 | 3731 | Missense Mutation | GGT,TGT | G,C 471 | XP_005246679.1 | |
XM_006712553.3 | 3731 | Missense Mutation | GGT,TGT | G,C 520 | XP_006712616.1 | |
XM_011511246.1 | 3731 | Missense Mutation | TGG,TTG | W,L 510 | XP_011509548.1 | |
XM_017004219.1 | 3731 | Missense Mutation | GGT,TGT | G,C 534 | XP_016859708.1 | |
XM_017004220.1 | 3731 | Missense Mutation | GGT,TGT | G,C 509 | XP_016859709.1 |