Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGACAAGACACCAGCGATCACGGCA[A/G]GATCCATGCAGTACTTTTGGCCAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LYG1 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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LYG1 - lysozyme g1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_174898.2 | 482 | Missense Mutation | CCT,CTT | P,L 83 | NP_777558.1 | |
XM_005263869.2 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_005263926.1 | |
XM_005263870.3 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_005263927.1 | |
XM_005263871.4 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_005263928.1 | |
XM_011510580.2 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_011508882.1 | |
XM_017003311.1 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_016858800.1 | |
XM_017003312.1 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_016858801.1 | |
XM_017003313.1 | 482 | Missense Mutation | CCT,CTT | P,L 83 | XP_016858802.1 |