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CCATAGGTCTGGCCCACGCTGAACC[A/G]AAGTAGTGGGCAGTGTCCAGTGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611053 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM166B 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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FAM166B - family with sequence similarity 166 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099951.3 | 159 | Missense Mutation | CGG,TGG | R,W 30 | NP_001093421.1 | |
NM_001164310.2 | 159 | Missense Mutation | CGG,TGG | R,W 30 | NP_001157782.1 | |
NM_001287238.1 | 159 | Missense Mutation | CGG,TGG | R,W 30 | NP_001274167.1 | |
NM_001287239.1 | 159 | Missense Mutation | CGG,TGG | R,W 30 | NP_001274168.1 | |
XM_011518028.2 | 159 | Missense Mutation | CGG,TGG | R,W 25 | XP_011516330.1 |
RUSC2 - RUN and SH3 domain containing 2 | ||||||
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There are no transcripts associated with this gene. |