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AATGGAAAGAGGCCAGAAGAGTATA[C/G]GGAAACCAGAAAAGATTATATTCTT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C4orf22 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) - 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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C4orf22 - chromosome 4 open reading frame 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206997.1 | Intron | NP_001193926.1 | ||||
NM_152770.2 | Intron | NP_689983.2 | ||||
XM_011531816.2 | Intron | XP_011530118.2 | ||||
XM_017007972.1 | Intron | XP_016863461.1 | ||||
XM_017007973.1 | Intron | XP_016863462.1 | ||||
XM_017007974.1 | Intron | XP_016863463.1 | ||||
XM_017007975.1 | Intron | XP_016863464.1 | ||||
XM_017007976.1 | Intron | XP_016863465.1 | ||||
XM_017007977.1 | Intron | XP_016863466.1 | ||||
XM_017007978.1 | Intron | XP_016863467.1 |
Set Membership: |
HapMap |