Genome Explorer
My Genome
Example genome — synthetic dataSearch and filter an example whole genome. Every result shows its evidence, its sources and when it was last reviewed.
Axolotl explains published evidence. It does not independently diagnose disease.
Genome summary
Total variants
38,42,193
Coding variants
24,618
Rare variants
7,942
ClinVar-linked variants
12,438
Genome build
GRCh38
Last analysis
24 Sep 2026
Variants
A curated set of 32 example variants from the synthetic genome
Filters (show variants matching all selected)
Showing variants changed in the September 2026 reanalysis
Showing all 32 variants
| Gene | Variant | Consequence | Frequency | Evidence | Interpretation | Updated |
|---|---|---|---|---|---|---|
| rs4244285 | p.Pro227=c.681G>A | Splice-altering synonymous | 21% | Strong | Evidence available | 18 Jul 2026 |
| rs12248560 | Non-codingc.-806C>T | Upstream (promoter) | 18% | Moderate | Evidence available | 18 Jul 2026 |
| rs4149056 | p.Val174Alac.521T>C | Missense | 11% | Strong | Evidence available | 12 Aug 2026 |
| rs1799853 | p.Arg144Cysc.430C>T | Missense | 6% | Strong | Evidence available | 30 Jun 2026 |
| rs9923231 | Non-codingc.-1639G>A | Upstream (promoter) | 37% | Strong | Evidence available | 30 Jun 2026 |
| rs3892097 | Splicec.506-1G>A | Splice acceptor | 12% | Strong | Evidence available | 12 Aug 2026 |
| rs776746 | Intronicc.219-237A>G | Intronic (splice-altering) | 68% | Strong | Educational example | 30 Jun 2026 |
| rs116855232 | p.Arg139Cysc.415C>T | Missense | 7% | Strong | Review recommended | 19 Sep 2026 |
| rs2231142 | p.Gln141Lysc.421C>A | Missense | 12% | Moderate | Evidence available | 12 Aug 2026 |
| rs762551 | Intronicc.-9-154C>A | Intronic | 62% | Limited | Educational example | 30 Jun 2026 |
| rs113993960 | p.Phe508delc.1521_1523del | In-frame deletion | 0.6% | Strong | Review recommended | 18 Jul 2026 |
| rs1800562 | p.Cys282Tyrc.845G>A | Missense | 3% | Strong | Evidence available | 18 Jul 2026 |
| rs1799945 | p.His63Aspc.187C>G | Missense | 9% | Conflicting | Conflicting interpretations | 12 Sep 2026 |
| novel | p.Leu373Valc.1117C>G | Missense | <0.01% | Limited | VUS | 19 Sep 2026 |
| rs1799966 | p.Ser1613Glyc.4837A>G | Missense | 34% | Strong | Likely benign | 30 Jun 2026 |
| rs16942 | p.Lys1183Argc.3548A>G | Missense | 33% | Strong | Likely benign | 30 Jun 2026 |
| rs144848 | p.Asn372Hisc.1114A>C | Missense | 26% | Strong | Likely benign | 30 Jun 2026 |
| novel | p.Leu2512Ilec.7534C>A | Missense | <0.01% | Limited | VUS | 19 Sep 2026 |
| rs1042522 | p.Pro72Argc.215C>G | Missense | 66% | Strong | Likely benign | 30 Jun 2026 |
| rs1061472 | p.Lys832Argc.2495A>G | Missense | 44% | Strong | Likely benign | 30 Jun 2026 |
| rs429358 | p.Cys130Argc.388T>C | Missense (position checked) | 15% | Strong | Educational example | 30 Jun 2026 |
| rs7412 | p.Arg176Cysc.526C>T | Missense | 8% | Strong | Educational example | 30 Jun 2026 |
| rs1801133 | p.Ala222Valc.665C>T | Missense | 25% | Conflicting | Conflicting interpretations | 12 Aug 2026 |
| rs4988235 | Intronicc.1917+326C>T | Intronic (regulatory) | 25% | Strong | Educational example | 30 Jun 2026 |
| rs1815739 | p.Arg577Terc.1729C>T | Stop gained (common) | 40% | Moderate | Educational example | 30 Jun 2026 |
| novel | p.Asp472Tyrc.1414G>T | Missense | 0.03% | Moderate | Likely benign | 21 Aug 2026 |
| novel | p.Arg1193Glnc.3578G>A | Missense | 0.4% | Limited | VUS | 19 Sep 2026 |
| novel | p.Pro20412Serc.61234C>T | Missense | 0.2% | Conflicting | Conflicting interpretations | 19 Sep 2026 |
| novel | p.Asp770Hisc.2308G>C | Missense | 0.01% | Limited | VUS | 21 Aug 2026 |
| novel | p.Thr2200Metc.6599C>T | Missense | 0.06% | Limited | Review recommended | 19 Sep 2026 |
| novel | p.Ala897=c.2690C>T | Synonymous | 0.3% | Moderate | Likely benign | 18 Jul 2026 |
| novel | Intronicc.7210-48G>A | Intronic | 0.8% | Limited | Educational example | 30 Jun 2026 |
No variants match
Try a gene such as BRCA2 or CYP2C19, an rsID, or a chromosome like chr17.
How results are labelled
- Evidence available
- Published evidence exists and is summarised with its sources.
- Review recommended
- Worth discussing with a genetics professional before drawing conclusions.
- Conflicting interpretations
- Sources disagree; all of them are shown.
- VUS
- Variant of uncertain significance. Not enough evidence either way; kept under review.
- Likely benign
- Evidence suggests no meaningful effect.
- Educational example
- Included to explain how genetics works, not as a health finding.