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CTACAGGGAAGAGCTGAGGGACCAC[C/T]GGAAGTACTGGTGCAGGAAGGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD300LG 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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CD300LG - CD300 molecule like family member g | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168322.1 | 579 | Silent Mutation | CGG,TGG | R,W 47 | NP_001161794.1 | |
NM_001168323.1 | 579 | Silent Mutation | CGG,TGG | R,W 47 | NP_001161795.1 | |
NM_001168324.1 | 579 | Silent Mutation | CGG,TGG | R,W 47 | NP_001161796.1 | |
NM_145273.3 | 579 | Silent Mutation | CGG,TGG | R,W 47 | NP_660316.2 | |
XM_005257075.2 | 579 | Silent Mutation | CGG,TGG | R,W 47 | XP_005257132.1 | |
XM_005257076.2 | 579 | Silent Mutation | CGG,TGG | R,W 47 | XP_005257133.1 | |
XM_006721721.2 | 579 | Missense Mutation | CGG,TGG | R,W 47 | XP_006721784.1 | |
XM_006721722.2 | 579 | Silent Mutation | CGG,TGG | R,W 47 | XP_006721785.1 | |
XM_011524384.2 | 579 | Silent Mutation | CGG,TGG | R,W 47 | XP_011522686.1 | |
XM_017024235.1 | 579 | Silent Mutation | CGG,TGG | R,W 47 | XP_016879724.1 |