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CCCCCATACCTCCAACTTCAGCATC[A/C]TGGTGACTTAATGCATCAATAGCTC
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 - 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 |
PRDM11 - PR domain 11 | ||||||
---|---|---|---|---|---|---|
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 |