Search by Variant

e.g. ALDH2_chr12_111761933_111822532, HBB_chr11_5220464_5232071.

Chromosome name (e.g., chr11).

Exact SnpEff gene name.

Target sampleid (e.g. HG02615).

Haplotype-annotation class (e.g., ahapid, ahapid+chapid).

Exact impact level (e.g., HIGH, MODERATE, LOW).

Keyword match in SnpEff annotation.

One or more haplotype IDs (comma-separated; e.g., a0001, a01, a0001c0001, a01c02, a1c2, a0001c0001t0005, a0001c0001t0005g0018).

Sample haplotype IDs to include (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

Haplotype IDs to exclude (comma-separated; e.g., a0001, a0002, a0001c0001, a0001c0001t0005, a1, a01).

Sample haplotype IDs to exclude (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

Start position (GRCh38).

End position (GRCh38).

Minimum alternate allele count (≥).

Maximum alternate allele count (≤).

Minimum variant length (≥).

Maximum variant length (≤).

Select column to sort.

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