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CCACAGGAGATGATGCTCGCTTTGG[A/T]ACTTAGGGCTAGAAAAAGTGTGGCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616727 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PHF21B 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)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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PHF21B - PHD finger protein 21B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135862.2 | Intron | NP_001129334.1 | ||||
NM_001242450.1 | Intron | NP_001229379.1 | ||||
NM_001284296.1 | Intron | NP_001271225.1 | ||||
NM_138415.4 | Intron | NP_612424.1 | ||||
XM_006724122.1 | Intron | XP_006724185.1 | ||||
XM_011529855.1 | Intron | XP_011528157.1 |