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GTGAAGACATCGTCGGTTCCTGGGG[A/G]CGAAGTCTCCTTGCTCCGCATCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 107310 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC9A1 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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SLC9A1 - solute carrier family 9 member A1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003047.4 | 2185 | Missense Mutation | CCC,TCC | P,S 771 | NP_003038.2 | |
XM_011542021.2 | 2185 | Missense Mutation | CCC,TCC | P,S 661 | XP_011540323.1 |