Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATTGTGGTGAATGAATTCTGCGAG[C/T]GCTTTTCCTATTATGGAATGAAAGG
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 - 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 |
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 | 322 | Missense Mutation | CGC,TGC | R,C 57 | NP_001139470.1 | |
NM_021082.3 | 322 | Missense Mutation | CGC,TGC | R,C 57 | NP_066568.3 | |
XM_005247722.3 | 322 | Missense Mutation | CGC,TGC | R,C 57 | XP_005247779.1 | |
XM_006713736.3 | 322 | Missense Mutation | CGC,TGC | R,C 57 | XP_006713799.1 | |
XM_017007074.1 | 322 | Missense Mutation | CGC,TGC | R,C 57 | XP_016862563.1 |