Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGCTTCTCTCCTGTGTGGATGCAC[C/T]GGTGAATGTGAAGGTTCGAGCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601069 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF239 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) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZNF239 - zinc finger protein 239 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099282.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001092752.1 | |
NM_001099283.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001092753.1 | |
NM_001099284.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001092754.1 | |
NM_001324347.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001311276.1 | |
NM_001324348.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001311277.1 | |
NM_001324349.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001311278.1 | |
NM_001324350.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001311279.1 | |
NM_001324351.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_001311280.1 | |
NM_001324352.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | NP_001311281.1 | |
NM_001324353.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 479 | NP_001311282.1 | |
NM_005674.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | NP_005665.2 | |
XM_005271832.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | XP_005271889.1 | |
XM_006718001.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_006718064.1 | |
XM_006718003.3 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | XP_006718066.1 | |
XM_011540232.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 510 | XP_011538534.1 | |
XM_011540234.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_011538536.1 | |
XM_011540235.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_011538537.1 | |
XM_011540236.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_011538538.1 | |
XM_011540237.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_011538539.1 | |
XM_011540238.2 | 1268 | Missense Mutation | CAG,CGG | Q,R 366 | XP_011538540.1 | |
XM_017016740.1 | 1268 | Missense Mutation | CAG,CGG | Q,R 408 | XP_016872229.1 |