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GGCATGGGCCGGGGCCTCTTGACCC[A/G]GAGGCCAGGCACGCGCAGAGGAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616587 MIM: 613622 MIM: 182180 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM118B 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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FAM118B - family with sequence similarity 118 member B | ||||||
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There are no transcripts associated with this gene. |
FOXRED1 - FAD dependent oxidoreductase domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017547.3 | 97 | Missense Mutation | CAG,CGG | Q,R 17 | NP_060017.1 | |
XM_006718879.3 | 97 | Intron | XP_006718942.1 | |||
XM_006718881.3 | 97 | UTR 5 | XP_006718944.1 | |||
XM_011542895.2 | 97 | UTR 5 | XP_011541197.1 | |||
XM_011542896.2 | 97 | UTR 5 | XP_011541198.1 | |||
XM_017018000.1 | 97 | Missense Mutation | CAG,CGG | Q,R 17 | XP_016873489.1 | |
XM_017018001.1 | 97 | UTR 5 | XP_016873490.1 | |||
XM_017018002.1 | 97 | UTR 5 | XP_016873491.1 | |||
XM_017018003.1 | 97 | UTR 5 | XP_016873492.1 | |||
XM_017018004.1 | 97 | UTR 5 | XP_016873493.1 | |||
XM_017018005.1 | 97 | Intron | XP_016873494.1 | |||
XM_017018006.1 | 97 | UTR 5 | XP_016873495.1 |
SRPRA - SRP receptor alpha subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177842.1 | 97 | Intron | NP_001171313.1 | |||
NM_003139.3 | 97 | Intron | NP_003130.2 | |||
XM_017018179.1 | 97 | Intron | XP_016873668.1 |