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TCTGCTCAAAACCCTCTACTATCTC[C/T]TATTTCACTCACAGTAAAATCCAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616703 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COMMD7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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COMMD7 - COMM domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099339.1 | Intron | NP_001092809.1 | ||||
NM_053041.2 | Intron | NP_444269.2 | ||||
XM_005260299.3 | Intron | XP_005260356.1 | ||||
XM_005260300.3 | Intron | XP_005260357.1 | ||||
XM_011528604.2 | Intron | XP_011526906.1 | ||||
XM_017027685.1 | Intron | XP_016883174.1 | ||||
XM_017027686.1 | Intron | XP_016883175.1 | ||||
XM_017027687.1 | Intron | XP_016883176.1 |