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GCGCCCAGCTACCATCACCATCACC[A/G]CCACCACCACCACCACCACCACCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600542 | ||||||||||||||||||||
Literature Links: |
LOC101928438 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 |
LOC101928438 - uncharacterized LOC101928438 | ||||||
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There are no transcripts associated with this gene. |
NR4A3 - nuclear receptor subfamily 4 group A member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006981.3 | 957 | Missense Mutation | CAC,CGC | H,R 99 | NP_008912.2 | |
NM_173199.2 | 957 | Missense Mutation | CAC,CGC | H,R 99 | NP_775291.1 | |
NM_173200.2 | 957 | Missense Mutation | CAC,CGC | H,R 110 | NP_775292.1 | |
XM_017015162.1 | 957 | Missense Mutation | CAC,CGC | H,R 99 | XP_016870651.1 |