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GTTCTTATCAGTCCAGTGGGTTTTT[A/C]TTTTACTTTAGTACACCATAATGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610091 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR4522 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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MIR4522 - microRNA 4522 | ||||||
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There are no transcripts associated with this gene. |
WSB1 - WD repeat and SOCS box containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015626.8 | Intron | NP_056441.6 | ||||
NM_134265.2 | Intron | NP_599027.1 | ||||
XM_005257963.3 | Intron | XP_005258020.1 | ||||
XM_017024433.1 | Intron | XP_016879922.1 | ||||
XM_017024434.1 | Intron | XP_016879923.1 | ||||
XM_017024435.1 | Intron | XP_016879924.1 | ||||
XM_017024436.1 | Intron | XP_016879925.1 |