EMD c.-7A>C
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP 0.29 | GERP -2.3 |
| Non-coding constraint | — | not assessed · autosomes only, so chrX has no window · absence ≠ unconstrained |
| Overall | ||
| CADD | 7.989 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- EMD
- Coding
- c.-7A>C
- MANE Select
- NM_000117
- dbSNP
- rs797044612
- Type
- single nucleotide variant
- Location
- chrX:154379478 (GRCh38)
- Structure
- AlphaFold pLDDT 61.26 · 6 PDB
Similar variants
- EMD c.187+1G>A Pathogenic ★★ same type
- EMD c.187+1G>T Pathogenic/Likely pathogenic ★★ same type
- EMD c.265+1G>A Likely pathogenic ★★ same type
- EMD c.265+2T>A Likely pathogenic ★★ same type
- EMD c.266-2A>G Pathogenic ★★ same type
- EMD c.266-3A>G Pathogenic ★★ same type
- EMD c.399+1G>T Pathogenic ★★ same type
- EMD c.399+2T>C Pathogenic ★★ same type
Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →
Cite Sugi Variant
Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/emd-c-minus-7a-c (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown