HRAS missense variants in ExAC

HRAS gene summary
HRAS variants in

The table below lists the HRAS missense variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord.✝ Variant (CDS)▼ Variant (Protein) Variant Type▼ ExAC frequency▼Populations*
1. 533799 c.257A>C p.N86T missense 0.00023154●●●●●●
2. 532686 c.520C>T p.P174S missense 0.00016814●●●●●●
3. 534312 c.11A>G p.Y4C missense 0.00005049●●●●●●
4. 532701 c.505C>T p.R169W missense 0.00004194●●●●●●
5. 533536 c.367C>T p.R123C missense 0.00003307●●●●●●
6. 532660 c.546G>A p.M182I missense 0.00002565●●●●●●
7. 532700 c.506G>A p.R169Q missense 0.00002517●●●●●●
8. 533535 c.368G>C p.R123P missense 0.00002480●●●●●●
9. 532668 c.538G>A p.G180S missense 0.00001696●●●●●●
10. 532746 c.460G>A p.D154N missense 0.00001675●●●●●●
11. 532716 c.490C>T p.R164W missense 0.00001674●●●●●●
12. 532724 c.482G>A p.R161H missense 0.00001674●●●●●●
13. 534292 c.31G>A p.A11T missense 0.00001669●●●●●●
14. 533803 c.253A>G p.N85D missense 0.00001654●●●●●●
15. 533606 c.297G>T p.Q99H missense 0.00001652●●●●●●
16. 532670 c.536C>T p.P179L missense 0.00000846●●●●●●
17. 532703 c.503T>C p.L168P missense 0.00000838●●●●●●
18. 532704 c.502C>G p.L168V missense 0.00000838●●●●●●
19. 532715 c.491G>A p.R164Q missense 0.00000837●●●●●●
20. 532725 c.481C>T p.R161C missense 0.00000837●●●●●●
21. 532715 c.491G>C p.R164P missense 0.00000837●●●●●●
22. 533485 c.418C>T p.P140S missense 0.00000829●●●●●●
23. 533491 c.412G>A p.G138S missense 0.00000829●●●●●●
24. 533477 c.426C>G p.I142M missense 0.00000829●●●●●●
25. 533944 c.112G>C p.D38H missense 0.00000829●●●●●●
26. 533776 c.280C>T p.H94Y missense 0.00000828●●●●●●
27. 533511 c.392A>G p.Q131R missense 0.00000828●●●●●●
28. 533496 c.407G>C p.S136T missense 0.00000828●●●●●●
29. 533505 c.398T>A p.L133H missense 0.00000828●●●●●●
30. 533509 c.394G>A p.D132N missense 0.00000828●●●●●●
31. 533538 c.365C>T p.A122V missense 0.00000827●●●●●●
32. 533527 c.376G>C p.E126Q missense 0.00000827●●●●●●
33. 533541 c.362C>T p.A121V missense 0.00000827●●●●●●
34. 533857 c.199A>G p.M67V missense 0.00000826●●●●●●
35. 533833 c.223G>A p.G75R missense 0.00000826●●●●●●
36. 533572 c.331A>G p.M111V missense 0.00000826●●●●●●
37. 533884 c.172A>C p.T58P missense 0.00000826●●●●●●
38. 533841 c.215T>G p.M72R missense 0.00000826●●●●●●
39. 533586 c.317C>T p.S106L missense 0.00000826●●●●●●
40. 533853 c.203G>A p.R68Q missense 0.00000826●●●●●●

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

✝ Genomic coordinates refer to the GRCh37 release of the human genome.