ClinVar Miner

List of variants in gene combination DHFR, MSH3 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_000791.4(DHFR):c.-259C>T rs6151597 0.00658
NM_000791.4(DHFR):c.-411G>A rs201149584 0.00430
NM_000791.4(DHFR):c.-443G>A rs577919981 0.00127
NM_002439.5(MSH3):c.225G>T (p.Leu75=) rs757491337 0.00047
NM_000791.4(DHFR):c.-349G>A rs146523896 0.00024
NM_000791.4(DHFR):c.-334T>G rs145429648 0.00009
NM_002439.5(MSH3):c.219C>T (p.Pro73=) rs778136308 0.00007
NM_002439.5(MSH3):c.171C>T (p.Ala57=) rs201906899 0.00005
NM_000791.4(DHFR):c.-379C>T rs772266495 0.00004
NM_002439.5(MSH3):c.146C>G (p.Pro49Arg) rs564858245 0.00004
NM_002439.5(MSH3):c.180C>T (p.Ala60=) rs748485429 0.00003
NM_002439.5(MSH3):c.198C>T (p.Pro66=) rs1435558278 0.00003
NM_002439.5(MSH3):c.117C>T (p.Ser39=) rs762866873 0.00002
NM_002439.5(MSH3):c.150C>G (p.Gly50=) rs774275160 0.00002
NM_002439.5(MSH3):c.216G>A (p.Pro72=) rs758709284 0.00002
NM_002439.5(MSH3):c.33C>T (p.Leu11=) rs564921007 0.00002
NM_002439.5(MSH3):c.57G>T (p.Ala19=) rs1447333327 0.00002
NM_000791.4(DHFR):c.-319G>A rs749586225 0.00001
NM_000791.4(DHFR):c.-391A>G rs910557064 0.00001
NM_002439.5(MSH3):c.114C>G (p.Ser38=) rs368081203 0.00001
NM_002439.5(MSH3):c.144C>T (p.Asp48=) rs747024539 0.00001
NM_002439.5(MSH3):c.186G>A (p.Ala62=) rs1561429048 0.00001
NM_002439.5(MSH3):c.195G>C (p.Ala65=) rs761734241 0.00001
NM_002439.5(MSH3):c.195G>T (p.Ala65=) rs761734241 0.00001
NM_002439.5(MSH3):c.222G>A (p.Gln74=) rs1279149249 0.00001
NM_002439.5(MSH3):c.231G>T (p.Pro77=) rs1435823219 0.00001
NM_002439.5(MSH3):c.24G>C (p.Ser8=) rs1320023097 0.00001
NM_002439.5(MSH3):c.93G>A (p.Thr31=) rs1271418564 0.00001
NM_000791.4(DHFR):c.-397C>G
NM_002439.5(MSH3):c.100C>T (p.Leu34=) rs2112797274
NM_002439.5(MSH3):c.102G>A (p.Leu34=)
NM_002439.5(MSH3):c.102G>C (p.Leu34=) rs559669988
NM_002439.5(MSH3):c.105A>G (p.Lys35=)
NM_002439.5(MSH3):c.108C>A (p.Ser36=)
NM_002439.5(MSH3):c.126T>C (p.Gly42=) rs1580538076
NM_002439.5(MSH3):c.126T>G (p.Gly42=)
NM_002439.5(MSH3):c.132C>A (p.Ala44=) rs749754328
NM_002439.5(MSH3):c.132C>G (p.Ala44=) rs749754328
NM_002439.5(MSH3):c.135C>A (p.Asp45Glu)
NM_002439.5(MSH3):c.135C>G (p.Asp45Glu)
NM_002439.5(MSH3):c.135C>T (p.Asp45=) rs972547684
NM_002439.5(MSH3):c.147T>C (p.Pro49=) rs1450213881
NM_002439.5(MSH3):c.147T>G (p.Pro49=)
NM_002439.5(MSH3):c.150C>A (p.Gly50=) rs774275160
NM_002439.5(MSH3):c.150C>T (p.Gly50=) rs774275160
NM_002439.5(MSH3):c.153T>G (p.Ala51=)
NM_002439.5(MSH3):c.156A>G (p.Ala52=) rs761607646
NM_002439.5(MSH3):c.156A>T (p.Ala52=)
NM_002439.5(MSH3):c.15G>A (p.Lys5=)
NM_002439.5(MSH3):c.165A>C (p.Ala55=)
NM_002439.5(MSH3):c.165A>G (p.Ala55=) rs2112797815
NM_002439.5(MSH3):c.165A>T (p.Ala55=)
NM_002439.5(MSH3):c.171C>A (p.Ala57=)
NM_002439.5(MSH3):c.171C>G (p.Ala57=) rs201906899
NM_002439.5(MSH3):c.174A>C (p.Ala58=) rs2112797977
NM_002439.5(MSH3):c.174A>T (p.Ala58=)
NM_002439.5(MSH3):c.177G>C (p.Ala59=) rs1464896652
NM_002439.5(MSH3):c.183A>C (p.Ala61=)
NM_002439.5(MSH3):c.183A>T (p.Ala61=)
NM_002439.5(MSH3):c.189C>G (p.Pro63=)
NM_002439.5(MSH3):c.189C>T (p.Pro63=) rs770922346
NM_002439.5(MSH3):c.192A>G (p.Pro64=)
NM_002439.5(MSH3):c.195G>A (p.Ala65=) rs761734241
NM_002439.5(MSH3):c.201A>C (p.Pro67=)
NM_002439.5(MSH3):c.204T>C (p.Ala68=)
NM_002439.5(MSH3):c.204T>G (p.Ala68=)
NM_002439.5(MSH3):c.207C>A (p.Pro69=) rs1422622213
NM_002439.5(MSH3):c.207C>T (p.Pro69=) rs1422622213
NM_002439.5(MSH3):c.208G>A (p.Ala70Thr) rs765698219
NM_002439.5(MSH3):c.210C>G (p.Ala70=) rs753160687
NM_002439.5(MSH3):c.219C>G (p.Pro73=) rs778136308
NM_002439.5(MSH3):c.225G>A (p.Leu75=) rs757491337
NM_002439.5(MSH3):c.225G>C (p.Leu75=)
NM_002439.5(MSH3):c.234C>T (p.His78=)
NM_002439.5(MSH3):c.234_235inv (p.Ile79Val)
NM_002439.5(MSH3):c.24G>A (p.Ser8=) rs1320023097
NM_002439.5(MSH3):c.27C>G (p.Gly9=)
NM_002439.5(MSH3):c.36T>A (p.Ala12=)
NM_002439.5(MSH3):c.36T>C (p.Ala12=) rs1749188879
NM_002439.5(MSH3):c.39C>T (p.Ala13=)
NM_002439.5(MSH3):c.42C>T (p.Ser14=)
NM_002439.5(MSH3):c.48A>T (p.Ser16=) rs976119718
NM_002439.5(MSH3):c.50C>T (p.Ala17Val) rs1749189749
NM_002439.5(MSH3):c.57G>A (p.Ala19=) rs1447333327
NM_002439.5(MSH3):c.60G>A (p.Arg20=) rs1416287946
NM_002439.5(MSH3):c.63A>G (p.Gln21=) rs1168176656
NM_002439.5(MSH3):c.66G>A (p.Ala22=) rs1580537815
NM_002439.5(MSH3):c.93G>C (p.Thr31=)

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