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TCAGCACAAAGTCGAAGTGTTCACG[C/G]AGGCCAAGGCCCCCCAGGATGCCCT
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 |
---|---|---|
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 |
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 | 1021 | Silent Mutation | CTC,CTG | L,L 150 | NP_001291438.1 | |
NM_001304510.1 | 1021 | Silent Mutation | CTC,CTG | L,L 150 | NP_001291439.1 | |
NM_001304511.1 | 1021 | Silent Mutation | CTC,CTG | L,L 150 | NP_001291440.1 | |
NM_031219.3 | 1021 | Silent Mutation | CTC,CTG | L,L 150 | NP_112496.1 |