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CTTCCGCGTGCTGAGGGCTATGGAC[A/G]CCTGTCACCGCCAGGGGCTGGCGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614218 | ||||||||||||||||||||
Literature Links: |
MIR22HG 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 |
MIR22HG - MIR22 host gene | ||||||
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There are no transcripts associated with this gene. |
WDR81 - WD repeat domain 81 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163673.1 | 946 | Intron | NP_001157145.1 | |||
NM_001163809.1 | 946 | Missense Mutation | ACC,GCC | T,A 273 | NP_001157281.1 | |
NM_001163811.1 | 946 | Intron | NP_001157283.1 | |||
NM_152348.3 | 946 | Intron | NP_689561.2 | |||
XM_011523651.2 | 946 | Intron | XP_011521953.1 | |||
XM_017024184.1 | 946 | Missense Mutation | ACC,GCC | T,A 273 | XP_016879673.1 |