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CCTCGAGAAGCACTAAGTCGGCTCC[A/G]GGAGCTCTGTCAACAGTGGCTACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616474 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PGBD1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PGBD1 - piggyBac transposable element derived 1 | ||||||
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There are no transcripts associated with this gene. |
ZSCAN26 - zinc finger and SCAN domain containing 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001023560.3 | 339 | Missense Mutation | CAG,CGG | Q,R 73 | NP_001018854.2 | |
NM_001111039.2 | 339 | Missense Mutation | CAG,CGG | Q,R 73 | NP_001104509.1 | |
NM_001287421.1 | 339 | Intron | NP_001274350.1 | |||
NM_001287422.1 | 339 | Intron | NP_001274351.1 | |||
NM_152736.5 | 339 | Intron | NP_689949.3 | |||
XM_011514862.2 | 339 | Missense Mutation | CAG,CGG | Q,R 73 | XP_011513164.1 | |
XM_011514864.1 | 339 | Missense Mutation | CAG,CGG | Q,R 44 | XP_011513166.1 | |
XM_011514866.1 | 339 | Intron | XP_011513168.1 | |||
XM_011514867.1 | 339 | UTR 5 | XP_011513169.1 | |||
XM_011514869.1 | 339 | UTR 5 | XP_011513171.1 | |||
XM_017011264.1 | 339 | Missense Mutation | CAG,CGG | Q,R 73 | XP_016866753.1 | |
XM_017011265.1 | 339 | UTR 5 | XP_016866754.1 |
Set Membership: |
HapMap |