Whole-exome sequencing identification of non-synonymous SNP variants of 10 CHI patients.
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https://figshare.com/articles/dataset/_Whole_exome_sequencing_identification_of_non_synonymous_SNP_variants_of_10_CHI_patients_/745521
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资源简介：
*Mutation reported in Human Genome Mutation Database( HGMD).
PolyPhen/SIFT: (−) benign or tolerated; (+) possibly damaging/DAMAGING Low confidence;
(++) probably damaging/DAMAGING.
In bold known causative genes.
创建时间：
2013-07-15
