Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613072 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOXHD1 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)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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LOXHD1 - lipoxygenase homology domains 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145472.2 | 2913 | Missense Mutation | GCC,GTC | A,V 987 | NP_001138944.1 | |
NM_001145473.2 | 2913 | Missense Mutation | GCC,GTC | A,V 337 | NP_001138945.1 | |
NM_001173129.1 | 2913 | Missense Mutation | GCC,GTC | A,V 337 | NP_001166600.1 | |
NM_001308013.1 | 2913 | Missense Mutation | GCC,GTC | A,V 891 | NP_001294942.1 | |
NM_144612.6 | 2913 | Missense Mutation | GCC,GTC | A,V 2036 | NP_653213.6 | |
XM_006722388.3 | 2913 | Missense Mutation | GCC,GTC | A,V 1031 | XP_006722451.1 | |
XM_006722389.3 | 2913 | Missense Mutation | GCC,GTC | A,V 987 | XP_006722452.1 | |
XM_006722390.3 | 2913 | Missense Mutation | GCC,GTC | A,V 987 | XP_006722453.1 | |
XM_006722391.3 | 2913 | Missense Mutation | GCC,GTC | A,V 969 | XP_006722454.1 | |
XM_011525804.2 | 2913 | Missense Mutation | GCC,GTC | A,V 1485 | XP_011524106.1 | |
XM_011525807.2 | 2913 | Missense Mutation | GCC,GTC | A,V 891 | XP_011524109.1 | |
XM_011525810.2 | 2913 | Missense Mutation | GCC,GTC | A,V 354 | XP_011524112.1 | |
XM_011525811.2 | 2913 | Missense Mutation | GCC,GTC | A,V 337 | XP_011524113.1 | |
XM_017025540.1 | 2913 | Missense Mutation | GCC,GTC | A,V 1750 | XP_016881029.1 | |
XM_017025541.1 | 2913 | Missense Mutation | GCC,GTC | A,V 1779 | XP_016881030.1 | |
XM_017025542.1 | 2913 | Intron | XP_016881031.1 | |||
XM_017025543.1 | 2913 | Intron | XP_016881032.1 | |||
XM_017025544.1 | 2913 | Intron | XP_016881033.1 | |||
XM_017025545.1 | 2913 | Intron | XP_016881034.1 | |||
XM_017025546.1 | 2913 | Intron | XP_016881035.1 | |||
XM_017025547.1 | 2913 | Intron | XP_016881036.1 | |||
XM_017025548.1 | 2913 | Missense Mutation | GCC,GTC | A,V 1892 | XP_016881037.1 |