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AAGGCGACAGGAGAGGGGCTGATCC[A/G]GGCCAAGGAGCCTGTGGACTGCGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611324 MIM: 611866 | ||||||||||||||||||||
Literature Links: |
CLSTN3 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 |
CLSTN3 - calsyntenin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014718.3 | 553 | Missense Mutation | CAG,CGG | Q,R 92 | NP_055533.2 | |
XM_006719163.3 | 553 | Missense Mutation | CAG,CGG | Q,R 104 | XP_006719226.1 |
RBP5 - retinol binding protein 5 | ||||||
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There are no transcripts associated with this gene. |