SnpEff
Annotates variants and predicts their localized structural and sequence ontology impacts.
What it does
Predicts up to 61% of distinct functional impacts when used in conjunction with auxiliary tools, standardizing genomic annotations.
STRC usage
Not yet tested on E1659A.
Connections
- STRC Variant c.4976A>C — Misha [see-also]
- STRC Gene [about]
[part-of]Tools index