Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602534 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRRC57 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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LRRC57 - leucine rich repeat containing 57 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153260.2 | 897 | Intron | NP_694992.2 | |||
XM_011521423.2 | 897 | UTR 3 | XP_011519725.1 | |||
XM_011521424.2 | 897 | Intron | XP_011519726.1 |
SNAP23 - synaptosome associated protein 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003825.3 | 897 | Silent Mutation | ACA,ACG | T,T 132 | NP_003816.2 | |
NM_130798.2 | 897 | Intron | NP_570710.1 | |||
XM_006720725.2 | 897 | Silent Mutation | ACA,ACG | T,T 143 | XP_006720788.1 | |
XM_017022692.1 | 897 | Silent Mutation | ACA,ACG | T,T 143 | XP_016878181.1 | |
XM_017022693.1 | 897 | Intron | XP_016878182.1 | |||
XM_017022694.1 | 897 | Intron | XP_016878183.1 |
Set Membership: |
HapMap |