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GGGGCCCCTGCTCAGGCAGTCCTGC[A/G]CCCACTGCCAGCGAGTCCCTCAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C16orf86 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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C16orf86 - chromosome 16 open reading frame 86 | ||||||
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There are no transcripts associated with this gene. |
ENKD1 - enkurin domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
GFOD2 - glucose-fructose oxidoreductase domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243650.1 | 902 | Intron | NP_001230579.1 | |||
NM_030819.3 | 902 | Silent Mutation | GGC,GGT | G,G 288 | NP_110446.3 | |
XM_006721288.3 | 902 | Silent Mutation | GGC,GGT | G,G 183 | XP_006721351.1 | |
XM_017023738.1 | 902 | Silent Mutation | GGC,GGT | G,G 288 | XP_016879227.1 |