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TACAGCCTAAGGAAGAAACCCTGCT[A/G]TGGGACTGTGGCTGCTCTGGACTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610054 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C5orf66 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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C5orf66 - chromosome 5 open reading frame 66 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277348.1 | 896 | Missense Mutation | TAT,TGT | Y,C 25 | NP_001264277.1 |
H2AFY - H2A histone family member Y | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040158.1 | 896 | Intron | NP_001035248.1 | |||
NM_004893.2 | 896 | Intron | NP_004884.1 | |||
NM_138609.2 | 896 | Intron | NP_613075.1 | |||
NM_138610.2 | 896 | Intron | NP_613258.2 | |||
XM_005272132.1 | 896 | Intron | XP_005272189.1 | |||
XM_005272134.3 | 896 | Intron | XP_005272191.1 | |||
XM_005272135.3 | 896 | Intron | XP_005272192.1 | |||
XM_011543729.2 | 896 | Intron | XP_011542031.1 | |||
XM_011543730.2 | 896 | Intron | XP_011542032.1 | |||
XM_011543731.1 | 896 | Intron | XP_011542033.1 | |||
XM_011543732.1 | 896 | Intron | XP_011542034.1 | |||
XM_011543733.2 | 896 | Intron | XP_011542035.1 | |||
XM_011543734.2 | 896 | Intron | XP_011542036.1 | |||
XM_011543735.2 | 896 | Intron | XP_011542037.1 | |||
XM_017010067.1 | 896 | Intron | XP_016865556.1 | |||
XM_017010068.1 | 896 | Intron | XP_016865557.1 | |||
XM_017010069.1 | 896 | Intron | XP_016865558.1 |