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TGCTTTCATTTGCCTTTTTGACCAC[C/T]TACTGTGTGCCACGCAATTCATATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614568 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UNC13C 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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UNC13C - unc-13 homolog C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005254394.4 | Intron | XP_005254451.1 | ||||
XM_017022220.1 | Intron | XP_016877709.1 | ||||
XM_017022221.1 | Intron | XP_016877710.1 | ||||
XM_017022222.1 | Intron | XP_016877711.1 | ||||
XM_017022223.1 | Intron | XP_016877712.1 | ||||
XM_017022224.1 | Intron | XP_016877713.1 | ||||
XM_017022225.1 | Intron | XP_016877714.1 |