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Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610790 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM117A 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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FAM117A - family with sequence similarity 117 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030802.3 | Intron | NP_110429.1 | ||||
XM_017025182.1 | Intron | XP_016880671.1 |
SLC35B1 - solute carrier family 35 member B1 | ||||||
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There are no transcripts associated with this gene. |