Curated dataset of 332 great apes. Deep sequencing (>= 12-fold per individual) data, mapped to the human genome (hg38). Joint variant calls (vcf) for autosomes and sex chromosomes. Data curation for p

NIAID Data Ecosystem30

Database mapping of SNVs found in the Malay individual.

群体遗传变异

遗传变异定位

$: Positioning of variations to genomic loci with respect to RefGene.*: Including indels.

Figshare2015-12-02 更新30

Supplementary Material for: Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans

血型系统遗传学

群体遗传变异

The U antigen (MNS5) is one of 49 antigens belonging to the MNS blood group system (ISBT002) carried on glycophorins A (GPA) and B (GPB). U is present on the red blood cells in almost all Europeans an

Figshare2020-01-21 更新40

gnomAD SNP variant counts

群体遗传变异

蛋白质编码SNP功能分析

This dataset contains variant counts at the resolution of individual amino acid positions as annotated by the gnomAD project. This file is required for running the COSMIS method.

Figshare2021-10-26 更新30

The 1KCIGP genomic variations

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