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CTAGTCTGGCTCCTCAGAAACATCT[A/G]GGGGCACAAGTGCAGCCTCTGCCCC
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 | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SLC12A7 - solute carrier family 12 member 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006598.2 | 4802 | UTR 3 | NP_006589.2 | |||
XM_005248231.3 | 4802 | UTR 3 | XP_005248288.1 | |||
XM_011513939.2 | 4802 | UTR 3 | XP_011512241.1 | |||
XM_011513940.2 | 4802 | UTR 3 | XP_011512242.1 | |||
XM_011513941.2 | 4802 | UTR 3 | XP_011512243.2 | |||
XM_017008958.1 | 4802 | UTR 3 | XP_016864447.1 | |||
XM_017008959.1 | 4802 | UTR 3 | XP_016864448.1 |