ClinVar Miner

List of variants in gene MRE11 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_005591.3(MRE11):c.*1083T>C rs118070493
NM_005591.3(MRE11):c.*1086A>G rs886048752
NM_005591.3(MRE11):c.*1304A>T rs562083257
NM_005591.3(MRE11):c.*1366G>A rs146641719
NM_005591.3(MRE11):c.*1554C>G rs886048751
NM_005591.3(MRE11):c.*1661A>C rs539061083
NM_005591.3(MRE11):c.*1776C>T rs104895005
NM_005591.3(MRE11):c.*189G>A rs151287483
NM_005591.3(MRE11):c.*1933G>T rs104895004
NM_005591.3(MRE11):c.*2067A>G rs13447755
NM_005591.3(MRE11):c.*2106T>C rs886048750
NM_005591.3(MRE11):c.*2178A>C rs886048749
NM_005591.3(MRE11):c.*2258G>C rs886048748
NM_005591.3(MRE11):c.*2296A>G rs886048747
NM_005591.3(MRE11):c.*2320T>C rs886048746
NM_005591.3(MRE11):c.*2444A>G rs369336016
NM_005591.3(MRE11):c.*2452C>T rs574670712
NM_005591.3(MRE11):c.*2662A>G rs13447759
NM_005591.3(MRE11):c.*2703A>G rs766297244
NM_005591.3(MRE11):c.*313G>A rs886048758
NM_005591.3(MRE11):c.*447T>G rs886048757
NM_005591.3(MRE11):c.*628G>A rs142407545
NM_005591.3(MRE11):c.*650_*659dupTCTCTCTCTC rs201800515
NM_005591.3(MRE11):c.*654_*659dupTCTCTC rs201800515
NM_005591.3(MRE11):c.*656_*659dupTCTC rs201800515
NM_005591.3(MRE11):c.*658_*659delTC rs201800515
NM_005591.3(MRE11):c.*658_*659dupTC rs201800515
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*660C>T rs591959
NM_005591.3(MRE11):c.*669C>G rs886048755
NM_005591.3(MRE11):c.*671C>T rs538218500
NM_005591.3(MRE11):c.*741A>G rs886048754
NM_005591.3(MRE11):c.*848A>G rs13447750
NM_005591.3(MRE11):c.*910dupT rs886048753
NM_005591.3(MRE11):c.*997A>G rs149208652
NM_005591.3(MRE11):c.-106+8C>T rs886048761
NM_005591.3(MRE11):c.1051C>T (p.Arg351Cys) rs757492041
NM_005591.3(MRE11):c.121G>A (p.Asp41Asn) rs116679717
NM_005591.3(MRE11):c.1225+10T>G rs863224734
NM_005591.3(MRE11):c.1238A>G (p.Asn413Ser) rs587782457
NM_005591.3(MRE11):c.1404T>C (p.Asp468=) rs368144567
NM_005591.3(MRE11):c.1463G>A (p.Arg488His) rs145377856
NM_005591.3(MRE11):c.1504C>T (p.Arg502Cys) rs186333183
NM_005591.3(MRE11):c.1545A>G (p.Glu515=) rs886048759
NM_005591.3(MRE11):c.1758G>A (p.Ser586=) rs766372720
NM_005591.3(MRE11):c.1783+7A>G rs774520952
NM_005591.3(MRE11):c.1853T>G (p.Met618Arg) rs748933763
NM_005591.3(MRE11):c.1858A>G (p.Ile620Val) rs144070976
NM_005591.3(MRE11):c.1868-4C>A rs768257868
NM_005591.3(MRE11):c.18A>T (p.Ala6=) rs758314845
NM_005591.3(MRE11):c.21-6_26delATATAGTGATGA rs587780138
NM_005591.3(MRE11):c.426C>T (p.Asp142=) rs3218740
NM_005591.3(MRE11):c.508C>A (p.Gln170Lys) rs587782030
NM_005591.3(MRE11):c.529G>A (p.Ala177Thr) rs142996063
NM_005591.3(MRE11):c.545-13A>G rs370306271
NM_005591.3(MRE11):c.585T>C (p.Asn195=) rs886048760
NM_005591.3(MRE11):c.822T>C (p.Leu274=) rs137868143
NM_005591.3(MRE11):c.848A>G (p.His283Arg) rs142727857
NM_005591.3(MRE11):c.914G>A (p.Arg305Gln) rs752483206

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