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TTTTAGGGGAGGGCTTTTTAAACAG[G/T]CCATTGAAATAAACGTAATCACAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613408 MIM: 613409 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC122 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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CCDC122 - coiled-coil domain containing 122 | ||||||
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There are no transcripts associated with this gene. |
LACC1 - laccase domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128303.1 | 757 | Missense Mutation | GCC,TCC | A,S 146 | NP_001121775.1 | |
NM_153218.2 | 757 | Missense Mutation | GCC,TCC | A,S 146 | NP_694950.2 | |
XM_005266261.3 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_005266318.1 | |
XM_006719766.3 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_006719829.1 | |
XM_006719767.3 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_006719830.1 | |
XM_011534933.2 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_011533235.1 | |
XM_011534934.2 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_011533236.1 | |
XM_011534935.2 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_011533237.1 | |
XM_017020394.1 | 757 | Missense Mutation | GCC,TCC | A,S 146 | XP_016875883.1 |