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CATCCTGGAGGGCAGCAGCTTTGCT[A/G]GCAAACGTATCTGGAAAAGGACAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607991 | ||||||||||||||||||||
Literature Links: |
SLC8A3 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 |
SLC8A3 - solute carrier family 8 member A3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130417.2 | 869 | Silent Mutation | NP_001123889.1 | |||
NM_033262.4 | 869 | Silent Mutation | NP_150287.1 | |||
NM_058240.3 | 869 | Silent Mutation | NP_489479.1 | |||
NM_182932.2 | 869 | Silent Mutation | NP_891977.1 | |||
NM_182936.2 | 869 | Silent Mutation | NP_891981.1 | |||
NM_183002.2 | 869 | Silent Mutation | NP_892114.1 | |||
XM_006720240.3 | 869 | Silent Mutation | XP_006720303.1 | |||
XM_017021606.1 | 869 | Silent Mutation | XP_016877095.1 | |||
XM_017021607.1 | 869 | Silent Mutation | XP_016877096.1 | |||
XM_017021608.1 | 869 | Silent Mutation | XP_016877097.1 | |||
XM_017021609.1 | 869 | Silent Mutation | XP_016877098.1 | |||
XM_017021610.1 | 869 | Intron | XP_016877099.1 | |||
XM_017021611.1 | 869 | Silent Mutation | XP_016877100.1 |