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TGTCTGCCGCCCTGGACGCTATTAC[A/G]AACAGCCAGATAATGGAGTCCTCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 182331 | ||||||||||||||||||||
Literature Links: |
ATP1B2 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 |
ATP1B2 - ATPase Na+/K+ transporting subunit beta 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303263.1 | 1035 | Missense Mutation | AAA,GAA | K,E 54 | NP_001290192.1 | |
NM_001678.4 | 1035 | Missense Mutation | AAA,GAA | K,E 136 | NP_001669.3 |