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dbSNP—Database for Single Nucleotide Polymorphisms and Other Classes of Minor Genetic Variation
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The human PIEZO1 residue corresponding to residue 1,835 is the site of a known, likely benign, missense variant within human populations that changes alanine to valine.
“It is also the site of a known, likely benign, missense variant within human populations that changes alanine to valine (Sherry et al. 1999).”
From RERconverge Expansion: Using Relative Evolutionary Rates to Study Complex Categorical Trait Evolution (2024) · cites this paper as Sherry et al. 1999
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Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
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- Altshul, 1990, J. Mol. Biol., 5, 403, 10.1016/S0022-2836(05)80360-2 · DOI · Paper page
- 10.1093/nar/27.1.12 · DOI
- 10.1038/ng0893-332 · DOI
- Collins, 1998, Genome Res., 8, 1229, 10.1101/gr.8.12.1229 · DOI
- 10.1006/geno.1998.5581 · DOI
- Masood, 1999, Nature., 398, 545, 10.1038/19126 · DOI
- 10.1126/science.2781285 · DOI
- 10.1007/s004390050932 · DOI
- Sherry, 1997, Genetics, 147, 1977, 10.1093/genetics/147.4.1977 · DOI
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Metadata
- Authors
- Sherry, S. T., Ward, M., & Sirotkin, K.
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 1999-08-01
- Volume
- 9
- Issue
- 8
- Pages
- 677-679
- ISSN
- 1088-9051
- 1549-5469
- Cited by
- 789
- References
- 1
- Language
- en
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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