ClinVar Miner

List of variants in gene MRE11 reported as likely pathogenic by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_005591.3(MRE11):c.1018-1G>A rs1555012083
NM_005591.3(MRE11):c.1098+2T>C rs876659343
NM_005591.3(MRE11):c.1225+1G>A rs876658665
NM_005591.3(MRE11):c.1226-2A>C rs1555009945
NM_005591.3(MRE11):c.154-1G>A rs1555017290
NM_005591.3(MRE11):c.1784-2A>G rs201572020
NM_005591.3(MRE11):c.1867+2T>C rs745677716
NM_005591.3(MRE11):c.1868-2A>C rs1555002450
NM_005591.3(MRE11):c.1926+2T>C rs1555002390
NM_005591.3(MRE11):c.1926+2_1926+5del rs1555002387
NM_005591.3(MRE11):c.1927-1G>T rs1295485913
NM_005591.3(MRE11):c.1927-2A>G rs587781822
NM_005591.3(MRE11):c.1960_1979dup (p.Lys661fs) rs587781442
NM_005591.3(MRE11):c.2070+2T>A rs786202801
NM_005591.3(MRE11):c.21-6_26del rs587780138
NM_005591.3(MRE11):c.315-2A>G rs876659145
NM_005591.3(MRE11):c.3G>T (p.Met1Ile) rs1555018818
NM_005591.3(MRE11):c.402+2_402+3delinsGGG rs1555015413
NM_005591.3(MRE11):c.545-1G>A rs1451215042
NM_005591.3(MRE11):c.660-1G>A rs876658917

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