Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCACTCATCGGACAGGCATGTGTT[A/G]CTCTTCTCTGACTGCTCTGTGGACC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
20 submissions
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Phenotype: |
MIM: 612866 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ALG14 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ALG14 - ALG14, UDP-N-acetylglucosaminyltransferase subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305242.1 | 520 | Intron | NP_001292171.1 | |||
NM_144988.3 | 520 | Intron | NP_659425.1 | |||
XM_005270582.3 | 520 | Intron | XP_005270639.1 | |||
XM_011540897.2 | 520 | Nonsense Mutation | CAA,TAA | Q,* 149 | XP_011539199.1 |
Set Membership: |
HapMap |