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GTGGCCTGGGGCTGGCCGGGGGAAG[A/G]GGAGATCCCGGGTTTGAGGGGCAGT
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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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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 | 2051 | Silent Mutation | CCC,CCT | P,P 408 | NP_110429.1 | |
XM_017025182.1 | 2051 | Silent Mutation | CCC,CCT | P,P 456 | XP_016880671.1 |
SLC35B1 - solute carrier family 35 member B1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |