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CTAGCCCCTCAGACAGAAGGGAAGA[G/T]GTCTCTCCAGGTGAGTCCATCCCCC
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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
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 | 3425 | Intron | NP_001138944.1 | |||
NM_001145473.2 | 3425 | Missense Mutation | ATC,CTC | I,L 508 | NP_001138945.1 | |
NM_001173129.1 | 3425 | Intron | NP_001166600.1 | |||
NM_001308013.1 | 3425 | Intron | NP_001294942.1 | |||
NM_144612.6 | 3425 | Missense Mutation | ATC,CTC | I,L 2207 | NP_653213.6 | |
XM_006722388.3 | 3425 | Missense Mutation | ATC,CTC | I,L 1202 | XP_006722451.1 | |
XM_006722389.3 | 3425 | Missense Mutation | ATC,CTC | I,L 1158 | XP_006722452.1 | |
XM_006722390.3 | 3425 | Missense Mutation | ATC,CTC | I,L 1158 | XP_006722453.1 | |
XM_006722391.3 | 3425 | Missense Mutation | ATC,CTC | I,L 1140 | XP_006722454.1 | |
XM_011525804.2 | 3425 | Missense Mutation | ATC,CTC | I,L 1656 | XP_011524106.1 | |
XM_011525807.2 | 3425 | Missense Mutation | ATC,CTC | I,L 1062 | XP_011524109.1 | |
XM_011525810.2 | 3425 | Missense Mutation | ATC,CTC | I,L 525 | XP_011524112.1 | |
XM_011525811.2 | 3425 | Missense Mutation | ATC,CTC | I,L 508 | XP_011524113.1 | |
XM_017025540.1 | 3425 | Missense Mutation | ATC,CTC | I,L 1921 | XP_016881029.1 | |
XM_017025541.1 | 3425 | Intron | XP_016881030.1 | |||
XM_017025542.1 | 3425 | Intron | XP_016881031.1 | |||
XM_017025543.1 | 3425 | Intron | XP_016881032.1 | |||
XM_017025544.1 | 3425 | Intron | XP_016881033.1 | |||
XM_017025545.1 | 3425 | Intron | XP_016881034.1 | |||
XM_017025546.1 | 3425 | Intron | XP_016881035.1 | |||
XM_017025547.1 | 3425 | Intron | XP_016881036.1 | |||
XM_017025548.1 | 3425 | Missense Mutation | ATC,CTC | I,L 2063 | XP_016881037.1 |