TTC19 c.302G>A
Uncertain significance
Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00932%, amr)
Conditions
1
Inborn genetic diseases
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| REVEL | 0.01 | strongly benign-leaning |
|---|---|---|
| Splicing | ||
| SpliceAI | — | not assessed · no allele here is in the release |
| Constraint at this position | ||
| Conservation | phyloP -0.67 | GERP -2.8 |
| Non-coding constraint | Z 3.07 | 1 kb window · o/e 0.79 · regional · uncalibrated |
| Overall | ||
| CADD | 5.102 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00932%
Admixed American · 5/53,668 alleles
Filtering AF
0.00615%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00567%
Overall
0.00635%
99/1,558,802 alleles · very rare
exomes 83/1,406,592 · genomes 16/152,210 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.00932% | 10,734 |
| European (non-Finnish) | 0.00742% | 13,474 |
| Ashkenazi Jewishnot grpmax-eligible | 0.00696% | 14,359 |
| African / African-American | 0.00541% | 18,488 |
| Remaining individualsnot grpmax-eligible | 0.00329% | 30,363 |
Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.
Variant & gene context
- Gene
- TTC19
- Coding
- c.302G>A
- MANE Select
- NM_017775
- dbSNP
- rs777492241
- Type
- single nucleotide variant
- Location
- chr17:15999787 (GRCh38)
- Gene constraint
- LOEUF 1.049 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 80.28
Similar variants
- TTC19 p.Ala200Val Uncertain significance ★★ ⚠ same condition
- TTC19 p.Ala263Ser Uncertain significance ★★ ⚠ same condition
- TTC19 p.Ala85Val Uncertain significance ★★ ⚠ same condition
- TTC19 p.Arg102Gly Uncertain significance ★★ ⚠ same condition
- TTC19 p.Arg124His Uncertain significance ★★ ⚠ same condition
- TTC19 p.Arg294Cys Uncertain significance ★★ ⚠ same condition
- TTC19 p.Ile206Met Uncertain significance ★★ ⚠ same condition
- TTC19 p.Lys160Gln Uncertain significance ★★ ⚠ same condition
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/ttc19-c-302g-a (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown