Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTCTTCCTCTCTGCTGTCCCCCTT[A/G]TGTGTCTGGAGCTCCGGCGTGGGAT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602155 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105379356 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)
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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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LOC105379356 - uncharacterized LOC105379356 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017014155.1 | 77 | Intron | XP_016869644.1 | |||
XM_017014156.1 | 77 | Intron | XP_016869645.1 |
UBXN8 - UBX domain protein 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282189.1 | 77 | Missense Mutation | ATG,GTG | M,V 18 | NP_001269118.1 | |
NM_001282199.1 | 77 | Missense Mutation | ATG,GTG | M,V 18 | NP_001269128.1 | |
NM_005671.3 | 77 | Missense Mutation | ATG,GTG | M,V 18 | NP_005662.1 | |
XM_011544655.2 | 77 | Intron | XP_011542957.1 | |||
XM_017013862.1 | 77 | Intron | XP_016869351.1 |