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CAGGGTTGGGGGTGGCAAGCAGCGG[A/G]ACGTGGTCACAGCGGGTAGGGGGTG
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) - 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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EFS - embryonal Fyn-associated substrate | ||||||
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There are no transcripts associated with this gene. |
SLC22A17 - solute carrier family 22 member 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289050.1 | 2034 | Silent Mutation | GTC,GTT | V,V 292 | NP_001275979.1 | |
NM_016609.4 | 2034 | Silent Mutation | GTC,GTT | V,V 510 | NP_057693.3 | |
NM_020372.3 | 2034 | Silent Mutation | GTC,GTT | V,V 528 | NP_065105.2 | |
XM_005267747.4 | 2034 | Silent Mutation | GTC,GTT | V,V 528 | XP_005267804.1 | |
XM_005267748.4 | 2034 | Silent Mutation | GTC,GTT | V,V 402 | XP_005267805.1 | |
XM_017021361.1 | 2034 | Silent Mutation | GTC,GTT | V,V 528 | XP_016876850.1 | |
XM_017021362.1 | 2034 | Silent Mutation | GTC,GTT | V,V 510 | XP_016876851.1 |
Set Membership: |
HapMap |