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GGAGATGAAGCCCCTGCTCCTGGCC[A/G]TCAGCCTTGGCCTCATTGCTGCCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 151675 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LCN1 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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LCN1 - lipocalin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252617.1 | 82 | Missense Mutation | ATC,GTC | I,V 8 | NP_001239546.1 | |
NM_001252618.1 | 82 | Missense Mutation | ATC,GTC | I,V 8 | NP_001239547.1 | |
NM_001252619.1 | 82 | Missense Mutation | ATC,GTC | I,V 8 | NP_001239548.1 | |
NM_002297.3 | 82 | Missense Mutation | ATC,GTC | I,V 8 | NP_002288.1 | |
XM_011518675.2 | 82 | Missense Mutation | ATC,GTC | I,V 72 | XP_011516977.1 |