NM_005591.4(MRE11):c.1286T>C (p.Val429Ala)
|
rs141293060
|
0.00023
|
NM_005591.4(MRE11):c.1643T>C (p.Ile548Thr)
|
rs373522639
|
0.00016
|
NM_005591.4(MRE11):c.1334A>G (p.Gln445Arg)
|
rs371730091
|
0.00014
|
NM_005591.4(MRE11):c.311G>C (p.Ser104Thr)
|
rs587780140
|
0.00011
|
NM_005591.4(MRE11):c.818C>G (p.Ser273Cys)
|
rs143400546
|
0.00009
|
NM_005591.4(MRE11):c.482A>G (p.Lys161Arg)
|
rs587782294
|
0.00007
|
NM_005591.4(MRE11):c.274G>A (p.Glu92Lys)
|
rs587780139
|
0.00006
|
NM_005591.4(MRE11):c.391G>A (p.Asp131Asn)
|
rs368403414
|
0.00006
|
NM_005591.4(MRE11):c.1972A>G (p.Thr658Ala)
|
rs587782756
|
0.00004
|
NM_005591.4(MRE11):c.476T>C (p.Val159Ala)
|
rs140130291
|
0.00003
|
NM_005591.4(MRE11):c.1139G>A (p.Arg380His)
|
rs587781646
|
0.00002
|
NM_005591.4(MRE11):c.1163G>A (p.Arg388Gln)
|
rs587780134
|
0.00002
|
NM_005591.4(MRE11):c.259C>T (p.Arg87Trp)
|
rs758112386
|
0.00002
|
NM_005591.4(MRE11):c.1154T>C (p.Phe385Ser)
|
rs786201817
|
0.00001
|
NM_005591.4(MRE11):c.1238A>G (p.Asn413Ser)
|
rs587782457
|
0.00001
|
NM_005591.4(MRE11):c.1478T>G (p.Leu493Arg)
|
rs786203158
|
0.00001
|
NM_005591.4(MRE11):c.1499A>T (p.Glu500Val)
|
rs786203159
|
0.00001
|
NM_005591.4(MRE11):c.1699A>G (p.Asn567Asp)
|
rs778585671
|
0.00001
|
NM_005591.4(MRE11):c.1718G>A (p.Gly573Glu)
|
rs587781461
|
0.00001
|
NM_005591.4(MRE11):c.1875A>C (p.Lys625Asn)
|
rs907660509
|
0.00001
|
NM_005591.4(MRE11):c.250A>G (p.Met84Val)
|
rs786203222
|
0.00001
|
NM_005591.4(MRE11):c.826C>T (p.Pro276Ser)
|
rs587782742
|
0.00001
|
NM_005591.4(MRE11):c.83A>C (p.Lys28Thr)
|
rs876658611
|
0.00001
|
NM_005591.4(MRE11):c.1007G>A (p.Cys336Tyr)
|
rs1228681022
|
|
NM_005591.4(MRE11):c.1185T>C (p.Ile395=)
|
rs1001831519
|
|
NM_005591.4(MRE11):c.1269A>C (p.Glu423Asp)
|
|
|
NM_005591.4(MRE11):c.1270G>A (p.Gly424Arg)
|
rs2135000168
|
|
NM_005591.4(MRE11):c.1462C>G (p.Arg488Gly)
|
rs375261439
|
|
NM_005591.4(MRE11):c.1526A>C (p.Gln509Pro)
|
rs1591667851
|
|
NM_005591.4(MRE11):c.1559G>C (p.Arg520Pro)
|
rs753148077
|
|
NM_005591.4(MRE11):c.1669G>A (p.Asp557Asn)
|
rs1591655152
|
|
NM_005591.4(MRE11):c.1724G>T (p.Gly575Val)
|
rs376555330
|
|
NM_005591.4(MRE11):c.1811G>A (p.Arg604His)
|
rs148637964
|
|
NM_005591.4(MRE11):c.1904T>G (p.Val635Gly)
|
rs780850078
|
|
NM_005591.4(MRE11):c.2071GAT[6] (p.Asp695dup)
|
rs779409748
|
|
NM_005591.4(MRE11):c.391G>T (p.Asp131Tyr)
|
rs368403414
|
|