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CCAGAGGACGAGTGCCCACTTGCTG[A/G]TCTTCACAGAGCACGCTGAAAGTAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607222 | ||||||||||||||||||||
Literature Links: |
ANKRD16 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 |
ANKRD16 - ankyrin repeat domain 16 | ||||||
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There are no transcripts associated with this gene. |
FBXO18 - F-box protein, helicase, 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258452.1 | 646 | Intron | NP_001245381.1 | |||
NM_001258453.1 | 646 | Intron | NP_001245382.1 | |||
NM_032807.4 | 646 | Missense Mutation | ATC,GTC | I,V 45 | NP_116196.3 | |
NM_178150.2 | 646 | Intron | NP_835363.1 | |||
XM_011519748.2 | 646 | Missense Mutation | ATC,GTC | I,V 45 | XP_011518050.1 | |
XM_017016842.1 | 646 | Missense Mutation | ATC,GTC | I,V 45 | XP_016872331.1 | |
XM_017016843.1 | 646 | Missense Mutation | ATC,GTC | I,V 45 | XP_016872332.1 | |
XM_017016844.1 | 646 | Intron | XP_016872333.1 | |||
XM_017016845.1 | 646 | Missense Mutation | ATC,GTC | I,V 45 | XP_016872334.1 | |
XM_017016846.1 | 646 | Intron | XP_016872335.1 |