ClinVar Miner

List of variants in gene MSH3 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002439.5(MSH3):c.1174-100T>C rs836807 0.99879
NM_002439.5(MSH3):c.1763+260T>C rs26266 0.87499
NM_002439.5(MSH3):c.2846A>G (p.Gln949Arg) rs184967 0.86544
NM_002439.5(MSH3):c.2543+140G>A rs33010 0.84296
NM_002439.5(MSH3):c.1763+240T>G rs26267 0.75860
NM_002439.5(MSH3):c.792+270A>T rs1650649 0.75844
NM_002439.5(MSH3):c.1341-79C>T rs245016 0.73496
NM_002439.5(MSH3):c.3133G>A (p.Ala1045Thr) rs26279 0.70269
NM_002439.5(MSH3):c.3001-239A>G rs245341 0.70221
NM_002439.5(MSH3):c.1897-204C>G rs33015 0.37815
NM_002439.5(MSH3):c.1453+61A>C rs32952 0.34979
NM_002439.5(MSH3):c.580-141G>T rs1650650 0.28006
NM_002439.5(MSH3):c.792+69G>A rs1677649 0.27979
NM_002439.5(MSH3):c.359-7G>A rs1382543 0.27946
NM_002439.5(MSH3):c.359-113A>G rs1650670 0.27945
NM_002439.5(MSH3):c.579+59G>A rs1824837 0.27942
NM_002439.5(MSH3):c.579+153C>T rs6151614 0.27931
NM_002439.5(MSH3):c.579+180G>A rs1824839 0.27930
NM_002439.5(MSH3):c.579+107G>A rs6151613 0.27892
NM_002439.5(MSH3):c.579+250G>T rs6151615 0.25998
NM_002439.5(MSH3):c.238-76G>A rs1382539 0.25750
NM_002439.5(MSH3):c.238-65C>G rs1382540 0.25745
NM_002439.5(MSH3):c.358+40T>C rs1643639 0.25735
NM_002439.5(MSH3):c.909+92A>G rs1677653 0.25402
NM_002439.5(MSH3):c.909+151G>A rs1677654 0.25396
NM_002439.5(MSH3):c.909+79T>A rs1650648 0.25377
NM_002439.5(MSH3):c.1340+71T>C rs836806 0.25352
NM_002439.5(MSH3):c.1174-176G>A rs836808 0.25344
NM_002439.5(MSH3):c.580-181T>C rs6151629 0.22911
NM_002439.5(MSH3):c.1454-236T>C rs245014 0.22887
NM_002439.5(MSH3):c.1341-104A>C rs32951 0.22856
NM_002439.5(MSH3):c.2656-145T>C rs2306371 0.15030
NM_002439.5(MSH3):c.2655+238A>G rs6151846 0.12633
NM_002439.5(MSH3):c.693G>A (p.Pro231=) rs1805355 0.12319
NM_002439.5(MSH3):c.579+288T>C rs6151616 0.12185
NM_002439.5(MSH3):c.1763+98A>G rs3816729 0.11961
NM_002439.5(MSH3):c.237+76G>T rs1677658 0.11739
NM_002439.5(MSH3):c.3131-262A>T rs6151927 0.11127
NM_002439.5(MSH3):c.3001-22T>A rs1805353 0.08582
NM_002439.5(MSH3):c.1654-146T>G rs7726620 0.03968
NM_002439.5(MSH3):c.1897-8A>G rs6151800 0.03966
NM_002439.5(MSH3):c.792+50G>A rs6151630 0.03852
NM_002439.5(MSH3):c.2814-251G>A rs6151912 0.03790
NM_002439.5(MSH3):c.359-136T>A rs182087282 0.03079
NM_002439.5(MSH3):c.2253+141_2253+143del rs56135406 0.02855
NM_002439.5(MSH3):c.3302+64G>A rs6151928 0.02435
NM_002439.5(MSH3):c.3302+70C>T rs6151929 0.01618
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.2685C>T (p.Thr895=) rs61753792 0.00024
NM_002439.5(MSH3):c.1174-12A>G rs202083881 0.00021
NM_002439.5(MSH3):c.3027C>G (p.Thr1009=) rs145319344 0.00019
NM_002439.5(MSH3):c.1341-220del rs33919693
NM_002439.5(MSH3):c.1341-221_1341-220del rs33919693
NM_002439.5(MSH3):c.1341-8del rs1580587338
NM_002439.5(MSH3):c.1453+11del
NM_002439.5(MSH3):c.1453+217C>A rs32953
NM_002439.5(MSH3):c.1454-5del rs780632399
NM_002439.5(MSH3):c.1569-5dup rs2112866721
NM_002439.5(MSH3):c.1653+275del rs6151747
NM_002439.5(MSH3):c.1764-8dup rs41559616
NM_002439.5(MSH3):c.1764-9_1764-8del rs41559616
NM_002439.5(MSH3):c.2318+145dup rs760266846
NM_002439.5(MSH3):c.2318+23dup
NM_002439.5(MSH3):c.237+249A>G rs6151599
NM_002439.5(MSH3):c.238-196A>G rs380691
NM_002439.5(MSH3):c.2544-88_2544-87del rs3830224
NM_002439.5(MSH3):c.2655+22dup
NM_002439.5(MSH3):c.2814-247C>T rs1979005
NM_002439.5(MSH3):c.3001-33_3001-30del rs3991216
NM_002439.5(MSH3):c.3130+214C>G rs6151919
NM_002439.5(MSH3):c.3303-7dup
NM_002439.5(MSH3):c.358+191C>G rs1677667
NM_002439.5(MSH3):c.358+76G>A rs1650694
NM_002439.5(MSH3):c.358+76G>C rs1650694
NM_002439.5(MSH3):c.579+106G>C rs6151612
NM_002439.5(MSH3):c.579+130C>A rs1824838
NM_002439.5(MSH3):c.793-109G>C rs1677652
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.