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GGAGACCTGGAAGCGCAGAACTCTC[A/C]GCATGAGAAGCTCACACTGCACGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300708 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM58A 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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FAM58A - family with sequence similarity 58 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130997.2 | 1014 | Intron | NP_001124469.1 | |||
NM_152274.4 | 1014 | Intron | NP_689487.2 | |||
XM_005277920.4 | 1014 | Intron | XP_005277977.1 | |||
XM_005277921.4 | 1014 | Intron | XP_005277978.1 | |||
XM_011531214.2 | 1014 | Missense Mutation | CGG,CTG | R,L 87 | XP_011529516.1 | |
XM_011531215.2 | 1014 | Missense Mutation | CGG,CTG | R,L 87 | XP_011529517.1 |
LOC105373383 - uncharacterized LOC105373383 | ||||||
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There are no transcripts associated with this gene. |