Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186360 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANXA7 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) - Not Available | ||||||
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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ANXA7 - annexin A7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001156.4 | 1397 | Missense Mutation | CAG,CGG | Q,R 419 | NP_001147.1 | |
NM_001320879.1 | 1397 | Missense Mutation | CAG,CGG | Q,R 379 | NP_001307808.1 | |
NM_001320880.1 | 1397 | Missense Mutation | CAG,CGG | Q,R 401 | NP_001307809.1 | |
NM_004034.3 | 1397 | Missense Mutation | CAG,CGG | Q,R 441 | NP_004025.1 | |
XM_017016162.1 | 1397 | Missense Mutation | CAG,CGG | Q,R 441 | XP_016871651.1 | |
XM_017016163.1 | 1397 | Missense Mutation | CAG,CGG | Q,R 419 | XP_016871652.1 |
Set Membership: |
HapMap |