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CTGAAGGGAGGAAGTAGAGGGAGCA[A/G]AAAATGGGAGGGAGGAAAGAAGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616347 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRDM11 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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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PRDM11 - PR domain 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256695.1 | Intron | NP_001243624.1 | ||||
NM_001256696.1 | Intron | NP_001243625.1 | ||||
XM_011520222.2 | Intron | XP_011518524.1 | ||||
XM_011520223.2 | Intron | XP_011518525.1 | ||||
XM_011520224.2 | Intron | XP_011518526.1 | ||||
XM_011520225.2 | Intron | XP_011518527.1 | ||||
XM_011520226.2 | Intron | XP_011518528.1 | ||||
XM_011520227.2 | Intron | XP_011518529.1 | ||||
XM_011520228.2 | Intron | XP_011518530.1 | ||||
XM_011520230.2 | Intron | XP_011518532.1 | ||||
XM_011520231.2 | Intron | XP_011518533.1 | ||||
XM_017018024.1 | Intron | XP_016873513.1 |