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GGGCCTCATCTCCCTCTATCTCACT[A/G]GCCTTTCTCTCATTCACTAACCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612636 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UNC80 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
UNC80 - unc-80 homolog, NALCN activator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032504.1 | Intron | NP_115893.1 | ||||
NM_182587.3 | Intron | NP_872393.3 | ||||
XM_005246476.1 | Intron | XP_005246533.1 | ||||
XM_011511004.1 | Intron | XP_011509306.1 | ||||
XM_011511005.1 | Intron | XP_011509307.1 | ||||
XM_011511006.1 | Intron | XP_011509308.1 | ||||
XM_011511007.1 | Intron | XP_011509309.1 | ||||
XM_011511008.1 | Intron | XP_011509310.1 | ||||
XM_011511010.2 | Intron | XP_011509312.1 | ||||
XM_011511012.1 | Intron | XP_011509314.1 | ||||
XM_017003884.1 | Intron | XP_016859373.1 | ||||
XM_017003885.1 | Intron | XP_016859374.1 | ||||
XM_017003886.1 | Intron | XP_016859375.1 | ||||
XM_017003887.1 | Intron | XP_016859376.1 | ||||
XM_017003888.1 | Intron | XP_016859377.1 | ||||
XM_017003889.1 | Intron | XP_016859378.1 | ||||
XM_017003890.1 | Intron | XP_016859379.1 | ||||
XM_017003891.1 | Intron | XP_016859380.1 | ||||
XM_017003892.1 | Intron | XP_016859381.1 | ||||
XM_017003893.1 | Intron | XP_016859382.1 | ||||
XM_017003894.1 | Intron | XP_016859383.1 |