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TCTCTGCACATGTATTTCTTTCTTC[C/T]TTTTCTCTATTGATTAATTTTTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608064 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLHL5 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
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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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KLHL5 - kelch like family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007075.2 | Intron | NP_001007076.1 | ||||
NM_001171654.1 | Intron | NP_001165125.1 | ||||
NM_015990.4 | Intron | NP_057074.3 | ||||
NM_199039.3 | Intron | NP_950240.2 | ||||
XM_005262655.4 | Intron | XP_005262712.1 | ||||
XM_011513699.2 | Intron | XP_011512001.1 | ||||
XM_011513700.2 | Intron | XP_011512002.1 | ||||
XM_011513701.2 | Intron | XP_011512003.1 | ||||
XM_017008273.1 | Intron | XP_016863762.1 | ||||
XM_017008274.1 | Intron | XP_016863763.1 | ||||
XM_017008275.1 | Intron | XP_016863764.1 | ||||
XM_017008276.1 | Intron | XP_016863765.1 |