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CCAGGAGGACTCTGTTCAGCCCCTC[A/G]GTCAGGACTTCAAGAAACTCCATGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604879 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC12A7 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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SLC12A7 - solute carrier family 12 member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006598.2 | 3252 | Silent Mutation | ACC,ACT | T,T 1062 | NP_006589.2 | |
XM_005248231.3 | 3252 | Silent Mutation | ACC,ACT | T,T 1067 | XP_005248288.1 | |
XM_011513939.2 | 3252 | Silent Mutation | ACC,ACT | T,T 1064 | XP_011512241.1 | |
XM_011513940.2 | 3252 | Silent Mutation | ACC,ACT | T,T 1053 | XP_011512242.1 | |
XM_011513941.2 | 3252 | Silent Mutation | ACC,ACT | T,T 1090 | XP_011512243.2 | |
XM_017008958.1 | 3252 | Silent Mutation | ACC,ACT | T,T 999 | XP_016864447.1 | |
XM_017008959.1 | 3252 | Silent Mutation | ACC,ACT | T,T 999 | XP_016864448.1 |