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TCCTGGAGGCCAGTCGTCCCGGCGC[G/T]GGGGCAGCTTGGCCACAGGCTCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610866 | ||||||||||||||||||||
Literature Links: |
UCKL1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
UCKL1-AS1 - UCKL1 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
ZNF512B - zinc finger protein 512B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020713.2 | 2716 | Missense Mutation | NP_065764.1 | |||
XM_005260226.3 | 2716 | Missense Mutation | XP_005260283.1 | |||
XM_011528929.2 | 2716 | Missense Mutation | XP_011527231.1 | |||
XM_011528930.2 | 2716 | Missense Mutation | XP_011527232.1 | |||
XM_011528931.2 | 2716 | Missense Mutation | XP_011527233.1 | |||
XM_011528932.2 | 2716 | Missense Mutation | XP_011527234.1 | |||
XM_011528933.2 | 2716 | Intron | XP_011527235.1 |