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CCAAAGCAAAGTTGACATAAAATTG[A/G]AGGCTATTTAGAAGAAGTGAATATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611527 MIM: 611789 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC9B1 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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SLC9B1 - solute carrier family 9 member B1 | ||||||
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There are no transcripts associated with this gene. |
SLC9B2 - solute carrier family 9 member B2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300754.1 | Intron | NP_001287683.1 | ||||
NM_001300756.1 | Intron | NP_001287685.1 | ||||
NM_178833.5 | Intron | NP_849155.2 | ||||
XM_006714085.2 | Intron | XP_006714148.1 | ||||
XM_006714086.3 | Intron | XP_006714149.1 |