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TTACCCGCAGCAGGAAGCCGTCGGG[A/G]CAGGTGAACTGGTCGTACCAGATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604647 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CALY 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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CALY - calcyon neuron specific vesicular protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321617.1 | 1641 | UTR 5 | NP_001308546.1 | |||
NM_015722.3 | 1641 | Silent Mutation | TGC,TGT | C,C 113 | NP_056537.1 | |
XM_005252685.4 | 1641 | Silent Mutation | TGC,TGT | C,C 146 | XP_005252742.2 | |
XM_011539836.2 | 1641 | Silent Mutation | TGC,TGT | C,C 146 | XP_011538138.1 | |
XM_011539838.2 | 1641 | Silent Mutation | TGC,TGT | C,C 26 | XP_011538140.1 |