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CTTGTGCTAACGGGTTAACTCCGTC[A/G]TACAGAACTCAGACTAAAACTCGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612377 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
COMMD6 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)
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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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COMMD6 - COMM domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287392.1 | 999 | UTR 3 | NP_001274321.1 | |||
NM_001287393.1 | 999 | UTR 3 | NP_001274322.1 | |||
NM_001287394.1 | 999 | UTR 3 | NP_001274323.1 | |||
NM_203495.3 | 999 | UTR 3 | NP_987091.1 | |||
NM_203497.3 | 999 | UTR 3 | NP_987093.1 | |||
XM_011534948.2 | 999 | Intron | XP_011533250.1 |