get_variant_effects
Lists per-transcript HGVS, consequence terms, and impact for a variant, prioritizing severe and MANE Select transcripts without frequencies or classification.
Instructions
List a variant's predicted molecular consequences on every overlapping transcript.
Returns per-transcript HGVS (c. and p.), consequence terms (e.g. missense_variant) and impact, most severe and MANE Select transcripts first. Lightweight: no frequencies or classification.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| genome | No | Genome build of coordinate input. | hg38 |
| variant | Yes | The variant, in any notation accepted by annotate_variant. |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| effects | Yes | ||
| variant | Yes | ||
| truncated | No | ||
| total_effects | Yes |