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GCAGAGAGCACAGGTAGAAGTCCGA[C/T]GGGCTCCCTCCTCCTCCCACAGGCT
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 |
---|---|---|
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 |
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 | 1506 | Silent Mutation | CCA,CCG | P,P 116 | NP_001275979.1 | |
NM_016609.4 | 1506 | Silent Mutation | CCA,CCG | P,P 334 | NP_057693.3 | |
NM_020372.3 | 1506 | Silent Mutation | CCA,CCG | P,P 334 | NP_065105.2 | |
XM_005267747.4 | 1506 | Silent Mutation | CCA,CCG | P,P 334 | XP_005267804.1 | |
XM_005267748.4 | 1506 | Intron | XP_005267805.1 | |||
XM_017021361.1 | 1506 | Silent Mutation | CCA,CCG | P,P 334 | XP_016876850.1 | |
XM_017021362.1 | 1506 | Silent Mutation | CCA,CCG | P,P 334 | XP_016876851.1 |