SnpEff

Annotates variants and predicts their localized structural and sequence ontology impacts.

Key Info

• URL: https://pcingola.github.io/SnpEff/
• Category: VEP
• API: Yes
• Free: Free
• ACMG Relevance: N/A
• Link Status: Unchecked

Why It Matters

Predicts up to 61% of distinct functional impacts when used in conjunction with auxiliary tools, standardizing genomic annotations.

STRC Research Usage

Not yet tested on E1659A.

Next Steps

• Verify URL accessibility
• Test with STRC E1659A variant if applicable
• Document specific results

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]