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AGCCAGGACTGCTCCTGAGCAACAC[C/T]GGGGGCACCTGCTCCAGGCCTTGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 104260 MIM: 608860 | ||||||||||||||||||||
Literature Links: |
ADRA2B 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 |
ADRA2B - adrenoceptor alpha 2B | ||||||
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There are no transcripts associated with this gene. |
ASTL - astacin-like metallo-endopeptidase (M12 family) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002036.3 | 1953 | Missense Mutation | AGT,GGT | S,G 380 | NP_001002036.3 | |
XM_011511205.2 | 1953 | Missense Mutation | AGT,GGT | S,G 385 | XP_011509507.1 | |
XM_011511206.2 | 1953 | Missense Mutation | AGT,GGT | S,G 381 | XP_011509508.1 | |
XM_011511207.2 | 1953 | Missense Mutation | AGT,GGT | S,G 367 | XP_011509509.1 | |
XM_011511208.2 | 1953 | Intron | XP_011509510.1 |