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GCCTGGCGGGCAACAGCTTCAGGCC[G/T]GAGCACAGGGCGCTGCTGAACGCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 120930 MIM: 609072 MIM: 612905 | ||||||||||||||||||||
Literature Links: |
C8G 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 |
C8G - complement component 8, gamma polypeptide | ||||||
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There are no transcripts associated with this gene. |
FBXW5 - F-box and WD repeat domain containing 5 | ||||||
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There are no transcripts associated with this gene. |
LCN12 - lipocalin 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178536.3 | 353 | Silent Mutation | CCG,CCT | P,P 55 | NP_848631.2 | |
XM_006717065.3 | 353 | Silent Mutation | CCG,CCT | P,P 55 | XP_006717128.1 | |
XM_011518560.2 | 353 | Silent Mutation | CCG,CCT | P,P 82 | XP_011516862.1 | |
XM_011518561.2 | 353 | Silent Mutation | CCG,CCT | P,P 83 | XP_011516863.2 | |
XM_011518562.2 | 353 | Silent Mutation | CCG,CCT | P,P 55 | XP_011516864.1 | |
XM_017014631.1 | 353 | Silent Mutation | CCG,CCT | P,P 83 | XP_016870120.1 | |
XM_017014632.1 | 353 | Silent Mutation | CCG,CCT | P,P 83 | XP_016870121.1 |