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GGTCAGGGGACCAAAATACACAACC[A/G]TCATAAAGATGAAGCTCTAGAGAAA
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 |
---|---|---|
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 |
FAM117A - family with sequence similarity 117 member A | ||||||
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There are no transcripts associated with this gene. |
SLC35B1 - solute carrier family 35 member B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278784.1 | 782 | Missense Mutation | ACG,ATG | T,M 193 | NP_001265713.1 | |
NM_005827.2 | 782 | Missense Mutation | ACG,ATG | T,M 297 | NP_005818.2 | |
XM_005256929.3 | 782 | Missense Mutation | ACG,ATG | T,M 193 | XP_005256986.1 | |
XM_006721632.3 | 782 | Missense Mutation | ACG,ATG | T,M 331 | XP_006721695.1 | |
XM_011524179.2 | 782 | Missense Mutation | ACG,ATG | T,M 254 | XP_011522481.1 | |
XM_011524180.2 | 782 | Missense Mutation | ACG,ATG | T,M 193 | XP_011522482.1 |