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GGAGTCTCCCCAACATGGCCTGCCC[A/G]GGCAGCACCCCGGCATGGTCCCCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615563 MIM: 604819 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR6845 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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MIR6845 - microRNA 6845 | ||||||
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There are no transcripts associated with this gene. |
NRBP2 - nuclear receptor binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178564.3 | 1779 | UTR 3 | NP_848659.2 | |||
XM_017013378.1 | 1779 | Missense Mutation | CGG,TGG | R,W 547 | XP_016868867.1 | |
XM_017013379.1 | 1779 | Missense Mutation | CGG,TGG | R,W 498 | XP_016868868.1 | |
XM_017013380.1 | 1779 | Missense Mutation | CGG,TGG | R,W 547 | XP_016868869.1 | |
XM_017013381.1 | 1779 | UTR 3 | XP_016868870.1 | |||
XM_017013382.1 | 1779 | Missense Mutation | CGG,TGG | R,W 547 | XP_016868871.1 | |
XM_017013383.1 | 1779 | Missense Mutation | CGG,TGG | R,W 498 | XP_016868872.1 |
PUF60 - poly(U) binding splicing factor 60 | ||||||
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There are no transcripts associated with this gene. |