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GGATGATATGAATGCAGGTGGGGAG[A/G]TCAAGGCTGGCCTAGTCCCGGGTGT
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) - 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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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 | Intron | NP_001275979.1 | ||||
NM_016609.4 | Intron | NP_057693.3 | ||||
NM_020372.3 | Intron | NP_065105.2 | ||||
XM_005267747.4 | Intron | XP_005267804.1 | ||||
XM_005267748.4 | Intron | XP_005267805.1 | ||||
XM_017021361.1 | Intron | XP_016876850.1 | ||||
XM_017021362.1 | Intron | XP_016876851.1 |