Search Thermo Fisher Scientific
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GTGTTACTGCCCCTTGGGGAAGAAC[A/G]GTTCTCCCTCCCCAGGCTCAGGGTG
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 |
---|---|---|
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 |
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 | 2300 | Missense Mutation | CCG,CTG | P,L 809 | NP_003038.2 | |
XM_011542021.2 | 2300 | Missense Mutation | CCG,CTG | P,L 699 | XP_011540323.1 |