FAVOR

Facilitates the annotation of variants based on their functional consequences.

What it does

Provides an easily integrated framework that significantly expands the total array of distinct functional impacts scored by primary VEPs.

How to use

See https://favor.genohub.org/ for documentation and access.

STRC usage

Not directly applicable to E1659A via API. Requires local installation or web interface. See documentation for manual usage.

Connections

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