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ATCTGAGCCGTGCTCCTTCTGGTGC[A/G]CTGAGATCTCCAGGGCATAGCTTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603889 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SIRPB1 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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SIRPB1 - signal regulatory protein beta 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005260641.3 | 1552 | Missense Mutation | XP_005260698.1 | |||
XM_005260643.3 | 1552 | Intron | XP_005260700.1 | |||
XM_005260644.3 | 1552 | Intron | XP_005260701.1 | |||
XM_011529130.2 | 1552 | Intron | XP_011527432.1 | |||
XM_011529134.2 | 1552 | Intron | XP_011527436.1 | |||
XM_017027577.1 | 1552 | Missense Mutation | XP_016883066.1 | |||
XM_017027578.1 | 1552 | Missense Mutation | XP_016883067.1 | |||
XM_017027579.1 | 1552 | Missense Mutation | XP_016883068.1 | |||
XM_017027580.1 | 1552 | Missense Mutation | XP_016883069.1 | |||
XM_017027581.1 | 1552 | Intron | XP_016883070.1 | |||
XM_017027582.1 | 1552 | Intron | XP_016883071.1 | |||
XM_017027583.1 | 1552 | Missense Mutation | XP_016883072.1 | |||
XM_017027584.1 | 1552 | Missense Mutation | XP_016883073.1 | |||
XM_017027585.1 | 1552 | Intron | XP_016883074.1 |