Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607659 MIM: 602339 | ||||||||||||||||||||||||||||||||
Literature Links: |
EAF2 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
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YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
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CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
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JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
EAF2 - ELL associated factor 2 | ||||||
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There are no transcripts associated with this gene. |
SLC15A2 - solute carrier family 15 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145998.1 | 294 | Silent Mutation | GCC,GCT | A,A 47 | NP_001139470.1 | |
NM_021082.3 | 294 | Silent Mutation | GCC,GCT | A,A 47 | NP_066568.3 | |
XM_005247722.3 | 294 | Silent Mutation | GCC,GCT | A,A 47 | XP_005247779.1 | |
XM_006713736.3 | 294 | Silent Mutation | GCC,GCT | A,A 47 | XP_006713799.1 | |
XM_017007074.1 | 294 | Silent Mutation | GCC,GCT | A,A 47 | XP_016862563.1 |
Set Membership: |
DME Validated Inventoried |