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AAGGGTTCATTCATTTATTCTTTCA[A/G]CAACTATTGGGCCGGGTGTGGTGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605836 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UNC13B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
UNC13B - unc-13 homolog B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006377.3 | Intron | NP_006368.3 | ||||
XM_011517681.2 | Intron | XP_011515983.1 | ||||
XM_011517682.2 | Intron | XP_011515984.1 | ||||
XM_011517683.2 | Intron | XP_011515985.1 | ||||
XM_011517684.2 | Intron | XP_011515986.1 | ||||
XM_011517685.2 | Intron | XP_011515987.1 | ||||
XM_011517686.2 | Intron | XP_011515988.1 | ||||
XM_017014191.1 | Intron | XP_016869680.1 | ||||
XM_017014192.1 | Intron | XP_016869681.1 |