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TTACAACAAATACCCAGATGCTGTG[G/T]CCACATGGCTAAACCCTGACCCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 166490 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPP1 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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SPP1 - secreted phosphoprotein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000582.2 | 286 | Missense Mutation | GCC,TCC | A,S 41 | NP_000573.1 | |
NM_001040058.1 | 286 | Missense Mutation | GCC,TCC | A,S 41 | NP_001035147.1 | |
NM_001040060.1 | 286 | Intron | NP_001035149.1 | |||
NM_001251829.1 | 286 | Intron | NP_001238758.1 | |||
NM_001251830.1 | 286 | Missense Mutation | GCC,TCC | A,S 54 | NP_001238759.1 | |
XM_017008564.1 | 286 | Missense Mutation | GCC,TCC | A,S 54 | XP_016864053.1 |