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TGGCTTCGAGCACCGCCACCTCCTC[A/G]GCCTGCTGAGCCTCCATGAGTGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 132880 MIM: 611810 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR2F6 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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NR2F6 - nuclear receptor subfamily 2 group F member 6 | ||||||
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There are no transcripts associated with this gene. |
USHBP1 - USH1 protein network component harmonin binding protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297703.1 | 2044 | Silent Mutation | GCC,GCT | A,A 609 | NP_001284632.1 | |
NM_001321417.1 | 2044 | Silent Mutation | GCC,GCT | A,A 673 | NP_001308346.1 | |
NM_031941.3 | 2044 | Silent Mutation | GCC,GCT | A,A 673 | NP_114147.2 | |
XM_011528351.2 | 2044 | Intron | XP_011526653.1 |