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GGTGTGGTGGTGCGTGTGCAGGTGC[C/T]GCTGGCCGAAGGGGGAGTGGCGATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF608 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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ZNF608 - zinc finger protein 608 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020747.2 | 3744 | Missense Mutation | CAG,CGG | Q,R 1458 | NP_065798.2 | |
XM_005272037.2 | 3744 | Missense Mutation | CAG,CGG | Q,R 1458 | XP_005272094.1 | |
XM_005272038.1 | 3744 | Missense Mutation | CAG,CGG | Q,R 1458 | XP_005272095.1 | |
XM_005272039.2 | 3744 | Missense Mutation | CAG,CGG | Q,R 1458 | XP_005272096.1 | |
XM_005272040.3 | 3744 | Missense Mutation | CAG,CGG | Q,R 1170 | XP_005272097.1 | |
XM_011543520.2 | 3744 | Intron | XP_011541822.1 | |||
XM_011543522.2 | 3744 | Missense Mutation | CAG,CGG | Q,R 1161 | XP_011541824.1 | |
XM_011543523.2 | 3744 | Missense Mutation | CAG,CGG | Q,R 1073 | XP_011541825.1 | |
XM_017009674.1 | 3744 | Missense Mutation | CAG,CGG | Q,R 1458 | XP_016865163.1 |