ClinVar Miner

List of variants in gene MSH3 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002439.5(MSH3):c.2846A>G (p.Gln949Arg) rs184967 0.86544
NM_002439.5(MSH3):c.3133G>A (p.Ala1045Thr) rs26279 0.70269
NM_002439.5(MSH3):c.359-7G>A rs1382543 0.27946
NM_002439.5(MSH3):c.238-76G>A rs1382539 0.25750
NM_002439.5(MSH3):c.693G>A (p.Pro231=) rs1805355 0.12319
NM_002439.5(MSH3):c.1897-8A>G rs6151800 0.03966
NM_002439.5(MSH3):c.1567G>A (p.Glu523Lys) rs34058399 0.00789
NM_002439.5(MSH3):c.2254-19T>G rs41562717 0.00405
NM_002439.5(MSH3):c.1896+18C>T rs150904071 0.00330
NM_002439.5(MSH3):c.2511G>A (p.Leu837=) rs149628160 0.00270
NM_002439.5(MSH3):c.2732T>G (p.Leu911Trp) rs41545019 0.00233
NM_002439.5(MSH3):c.1571A>C (p.Asn524Thr) rs55724159 0.00220
NM_002439.5(MSH3):c.1469C>A (p.Ser490Tyr) rs76249824 0.00201
NM_002439.5(MSH3):c.1887T>C (p.Tyr629=) rs139201310 0.00193
NM_002439.5(MSH3):c.2480A>G (p.His827Arg) rs138339194 0.00191
NM_002439.5(MSH3):c.1897-12T>A rs56244266 0.00171
NM_002439.5(MSH3):c.1992G>A (p.Gln664=) rs144019582 0.00143
NM_002439.5(MSH3):c.792+8G>A rs147777411 0.00136
NM_002439.5(MSH3):c.1794G>A (p.Ser598=) rs61753791 0.00130
NM_002439.5(MSH3):c.2318+11A>G rs200378976 0.00111
NM_002439.5(MSH3):c.1453+15T>C rs200717987 0.00096
NM_002439.5(MSH3):c.356C>T (p.Ser119Phe) rs144607594 0.00028
NM_002439.5(MSH3):c.1174-12A>G rs202083881 0.00021
NM_002439.5(MSH3):c.1341-8del rs1580587338
NM_002439.5(MSH3):c.1453+11del
NM_002439.5(MSH3):c.1454-5del rs780632399
NM_002439.5(MSH3):c.1569-5dup rs2112866721
NM_002439.5(MSH3):c.1764-8dup rs41559616
NM_002439.5(MSH3):c.1764-9_1764-8del rs41559616
NM_002439.5(MSH3):c.2318+23dup
NM_002439.5(MSH3):c.2655+22dup
NM_002439.5(MSH3):c.3303-7dup
NM_002439.5(MSH3):c.793-11del
NM_002439.5(MSH3):c.793-3del rs754475791
NM_002439.5(MSH3):c.793-3dup rs754475791

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.