Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609906 MIM: 611461 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
EFS 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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EFS - embryonal Fyn-associated substrate | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277174.1 | 1461 | Missense Mutation | ATG,GTG | M,V 285 | NP_001264103.1 | |
NM_005864.3 | 1461 | Missense Mutation | ATG,GTG | M,V 454 | NP_005855.1 | |
NM_032459.2 | 1461 | Missense Mutation | ATG,GTG | M,V 361 | NP_115835.1 | |
XM_005267256.1 | 1461 | Missense Mutation | ATG,GTG | M,V 424 | XP_005267313.1 |
SLC22A17 - solute carrier family 22 member 17 | ||||||
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There are no transcripts associated with this gene. |