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GGCTTTCTGTGAGGATGAGCAGCAC[A/C]GGGATAGACAGGAAGGGCGTCCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615194 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHRS2 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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DHRS2 - dehydrogenase/reductase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318835.1 | 200 | Silent Mutation | ACA,ACC | T,T 26 | NP_001305764.1 | |
NM_005794.3 | 200 | Silent Mutation | ACA,ACC | T,T 26 | NP_005785.1 | |
NM_182908.4 | 200 | Silent Mutation | ACA,ACC | T,T 26 | NP_878912.1 | |
XM_005267249.1 | 200 | Silent Mutation | ACA,ACC | T,T 26 | XP_005267306.1 | |
XM_006720001.3 | 200 | Silent Mutation | ACA,ACC | T,T 26 | XP_006720064.1 | |
XM_011536338.1 | 200 | Intron | XP_011534640.1 | |||
XM_011536339.2 | 200 | Intron | XP_011534641.1 |