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TATTTTTATCTGAAATTTTAATTTA[A/G]ACGTACTTATTTTTAGAAGAGTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614161 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRDM5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
PRDM5 - PR domain 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300823.1 | Intron | NP_001287752.1 | ||||
NM_001300824.1 | Intron | NP_001287753.1 | ||||
NM_018699.3 | Intron | NP_061169.2 | ||||
XM_005262708.3 | Intron | XP_005262765.1 | ||||
XM_011531562.2 | Intron | XP_011529864.1 | ||||
XM_011531563.2 | Intron | XP_011529865.1 | ||||
XM_011531564.2 | Intron | XP_011529866.1 | ||||
XM_011531565.2 | Intron | XP_011529867.1 | ||||
XM_011531566.2 | Intron | XP_011529868.1 | ||||
XM_011531567.2 | Intron | XP_011529869.1 | ||||
XM_011531568.2 | Intron | XP_011529870.1 | ||||
XM_011531569.2 | Intron | XP_011529871.1 | ||||
XM_011531570.2 | Intron | XP_011529872.1 | ||||
XM_017007668.1 | Intron | XP_016863157.1 | ||||
XM_017007669.1 | Intron | XP_016863158.1 | ||||
XM_017007670.1 | Intron | XP_016863159.1 | ||||
XM_017007671.1 | Intron | XP_016863160.1 |