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GTACAGCTGAAGGAGGAAGGAAACC[A/G]GCATTTCCAGCTCCAGGACTACAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611220 | ||||||||||||||||||||
Literature Links: |
NLE1 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 |
NLE1 - notchless homolog 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
UNC45B - unc-45 myosin chaperone B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033576.1 | 44 | Missense Mutation | CAG,CGG | Q,R 15 | NP_001028748.1 | |
NM_001267052.1 | 44 | Missense Mutation | CAG,CGG | Q,R 15 | NP_001253981.1 | |
NM_001308281.1 | 44 | Missense Mutation | CAG,CGG | Q,R 15 | NP_001295210.1 | |
NM_173167.3 | 44 | Missense Mutation | CAG,CGG | Q,R 15 | NP_775259.1 | |
XM_017024234.1 | 44 | Missense Mutation | CAG,CGG | Q,R 15 | XP_016879723.1 |