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CGCTTGAAGCCAGATGAAAACCTTA[A/G]GCTGGGGAAATGATGATACTGATAG
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
COMMD7 - COMM domain containing 7 | ||||||
---|---|---|---|---|---|---|
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 |