Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCTCTCAGCAAAGAAGGCAGGGC[A/G]GTTCAGGGCACACTGCACTGCAAGT
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) - 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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ANXA7 - annexin A7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001156.4 | 1324 | Missense Mutation | CGC,TGC | R,C 395 | NP_001147.1 | |
NM_001320879.1 | 1324 | Missense Mutation | CGC,TGC | R,C 355 | NP_001307808.1 | |
NM_001320880.1 | 1324 | Missense Mutation | CGC,TGC | R,C 377 | NP_001307809.1 | |
NM_004034.3 | 1324 | Missense Mutation | CGC,TGC | R,C 417 | NP_004025.1 | |
XM_017016162.1 | 1324 | Missense Mutation | CGC,TGC | R,C 417 | XP_016871651.1 | |
XM_017016163.1 | 1324 | Missense Mutation | CGC,TGC | R,C 395 | XP_016871652.1 |