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TTCTTGCCAAAGACTCGCCTCAGTT[A/C]CTGAGACCCCCAGTGTGCTGGACGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613621 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NUBPL 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
|
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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NUBPL - nucleotide binding protein like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201573.1 | Intron | NP_001188502.1 | ||||
NM_001201574.1 | Intron | NP_001188503.1 | ||||
NM_025152.2 | Intron | NP_079428.2 | ||||
XM_011537181.2 | Intron | XP_011535483.1 | ||||
XM_011537182.2 | Intron | XP_011535484.1 | ||||
XM_011537183.2 | Intron | XP_011535485.1 | ||||
XM_011537184.2 | Intron | XP_011535486.1 | ||||
XM_017021664.1 | Intron | XP_016877153.1 | ||||
XM_017021665.1 | Intron | XP_016877154.1 | ||||
XM_017021666.1 | Intron | XP_016877155.1 | ||||
XM_017021667.1 | Intron | XP_016877156.1 |