ClinVar Miner

List of variants in gene CARS2 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024537.4(CARS2):c.1054+8G>A rs374859 0.00434
NM_024537.4(CARS2):c.1417-17C>T rs113709957 0.00417
NM_024537.4(CARS2):c.465+14C>T rs41315944 0.00061
NM_024537.4(CARS2):c.1318-18C>T rs185912329 0.00034
NM_024537.4(CARS2):c.571+11T>C rs373960867 0.00031
NM_024537.4(CARS2):c.466-18G>A rs370423607 0.00013
NM_024537.4(CARS2):c.1194-17C>G rs377292484 0.00009
NM_024537.4(CARS2):c.1503G>A (p.Ala501=) rs753425826 0.00007
NM_024537.4(CARS2):c.1608C>T (p.His536=) rs748996703 0.00005
NM_024537.4(CARS2):c.1011C>T (p.Pro337=) rs142857490 0.00004
NM_024537.4(CARS2):c.1407A>C (p.Ala469=) rs780686611 0.00004
NM_024537.4(CARS2):c.528T>C (p.Ile176=) rs759194567 0.00003
NM_024537.4(CARS2):c.920-18C>A rs1057521365 0.00003
NM_024537.4(CARS2):c.1689G>A (p.Ala563=) rs774357584 0.00002
NM_024537.4(CARS2):c.855C>T (p.Asn285=) rs201463850 0.00002
NM_024537.4(CARS2):c.1008C>T (p.Ser336=) rs1313306865 0.00001
NM_024537.4(CARS2):c.1257G>A (p.Val419=) rs774758878 0.00001
NM_024537.4(CARS2):c.1473G>A (p.Val491=) rs774705663 0.00001
NM_024537.4(CARS2):c.744C>T (p.Pro248=) rs747726067 0.00001
NM_024537.4(CARS2):c.1623+17G>A rs550431344
NM_024537.4(CARS2):c.354T>C (p.Ile118=)
NM_024537.4(CARS2):c.920-18C>T rs1057521365

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.