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CCGGCTTGGGCCAGCCAGCAGCCTC[A/G]GAGGTCAGCACAAAGTCGAAGTGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
BSPRY 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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BSPRY - B-box and SPRY domain containing | ||||||
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There are no transcripts associated with this gene. |
HDHD3 - haloacid dehalogenase like hydrolase domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304509.1 | 1051 | Silent Mutation | TCC,TCT | S,S 160 | NP_001291438.1 | |
NM_001304510.1 | 1051 | Silent Mutation | TCC,TCT | S,S 160 | NP_001291439.1 | |
NM_001304511.1 | 1051 | Silent Mutation | TCC,TCT | S,S 160 | NP_001291440.1 | |
NM_031219.3 | 1051 | Silent Mutation | TCC,TCT | S,S 160 | NP_112496.1 |