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GCCCAACTCCTGGGAAACATCTCTC[C/T]GCTGCATGGCCCGGAACCCCACTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
58 submissions
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Phenotype: |
MIM: 600684 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105371470 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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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC105371470 - uncharacterized LOC105371470 | ||||||
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There are no transcripts associated with this gene. |
LY9 - lymphocyte antigen 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033667.2 | 158 | Intron | NP_001028839.1 | |||
NM_001261456.1 | 158 | Intron | NP_001248385.1 | |||
NM_001261457.1 | 158 | Intron | NP_001248386.1 | |||
NM_002348.3 | 158 | Intron | NP_002339.2 | |||
XM_011509548.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507850.1 | |
XM_011509549.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507851.1 | |
XM_011509550.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507852.1 | |
XM_011509552.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507854.1 | |
XM_011509556.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507858.1 | |
XM_011509560.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_011507862.1 | |
XM_017001297.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_016856786.1 | |
XM_017001298.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_016856787.1 | |
XM_017001299.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_016856788.1 | |
XM_017001300.1 | 158 | Intron | XP_016856789.1 | |||
XM_017001301.1 | 158 | Intron | XP_016856790.1 | |||
XM_017001302.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_016856791.1 | |
XM_017001303.1 | 158 | Missense Mutation | CCG,CTG | P,L 42 | XP_016856792.1 | |
XM_017001304.1 | 158 | Intron | XP_016856793.1 |
Set Membership: |
HapMap |