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GCTGTAGATGGCGTTCTCGCGCTGG[C/T]GCTTGAAGAGCCGCACCCAGACGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614910 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C1QTNF6 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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C1QTNF6 - C1q and tumor necrosis factor related protein 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031910.3 | 3323 | Missense Mutation | NP_114116.3 | |||
NM_182486.1 | 3323 | Missense Mutation | NP_872292.1 | |||
XM_011529857.1 | 3323 | Missense Mutation | XP_011528159.1 | |||
XM_017028569.1 | 3323 | Missense Mutation | XP_016884058.1 | |||
XM_017028570.1 | 3323 | Missense Mutation | XP_016884059.1 | |||
XM_017028571.1 | 3323 | Missense Mutation | XP_016884060.1 | |||
XM_017028572.1 | 3323 | Missense Mutation | XP_016884061.1 | |||
XM_017028573.1 | 3323 | Missense Mutation | XP_016884062.1 | |||
XM_017028574.1 | 3323 | Missense Mutation | XP_016884063.1 |