Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608396 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC9A9 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SLC9A9 - solute carrier family 9 member A9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173653.3 | 1974 | Missense Mutation | ATA,GTA | I,V 589 | NP_775924.1 | |
XM_011512703.2 | 1974 | Missense Mutation | ATA,GTA | I,V 373 | XP_011511005.1 | |
XM_011512704.2 | 1974 | Intron | XP_011511006.1 | |||
XM_017006202.1 | 1974 | Intron | XP_016861691.1 | |||
XM_017006203.1 | 1974 | Missense Mutation | ATA,GTA | I,V 472 | XP_016861692.1 |
Set Membership: |
HapMap |