Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.94476344T>ACA382376809MRE11c.604A>T (p.Arg202Ter)
c.613A>T (p.Arg205Ter)
c.136A>T (p.Arg46Ter)
n.900A>T
11g.94476344T>CCA288181MRE11c.604A>G (p.Arg202Gly)
c.613A>G (p.Arg205Gly)
c.136A>G (p.Arg46Gly)
n.900A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.94476344T>GCA476286760MRE11c.604A>C (p.Arg202=)
c.613A>C (p.Arg205=)
c.136A>C (p.Arg46=)
n.900A>C
11g.94476344T=CA1992433230MRE11c.604A= (p.Arg202=)
c.613A= (p.Arg205=)
c.136A= (p.Arg46=)
n.900A=
11g.94476345C>ACA382376814MRE11c.603G>T (p.Leu201Phe)
c.612G>T (p.Leu204Phe)
c.135G>T (p.Leu45Phe)
n.899G>T
11g.94476345C>GCA382376816MRE11c.603G>C (p.Leu201Phe)
c.612G>C (p.Leu204Phe)
c.135G>C (p.Leu45Phe)
n.899G>C
11g.94476345C>TCA476286761MRE11c.603G>A (p.Leu201=)
c.612G>A (p.Leu204=)
c.135G>A (p.Leu45=)
n.899G>A
11g.94476346A>CCA382376818MRE11c.602T>G (p.Leu201Trp)
c.611T>G (p.Leu204Trp)
c.134T>G (p.Leu45Trp)
n.898T>G
 ClinVar
11g.94476346A>GCA382376821MRE11c.602T>C (p.Leu201Ser)
c.611T>C (p.Leu204Ser)
c.134T>C (p.Leu45Ser)
n.898T>C
11g.94476346A>TCA382376823MRE11c.602T>A (p.Leu201Ter)
c.611T>A (p.Leu204Ter)
c.134T>A (p.Leu45Ter)
n.898T>A
11g.94476347A>CCA382376825MRE11c.601T>G (p.Leu201Val)
c.610T>G (p.Leu204Val)
c.133T>G (p.Leu45Val)
n.897T>G
11g.94476347A>GCA476286762MRE11c.601T>C (p.Leu201=)
c.610T>C (p.Leu204=)
c.133T>C (p.Leu45=)
n.897T>C
 gnomAD v4
11g.94476347A>TCA382376828MRE11c.601T>A (p.Leu201Met)
c.610T>A (p.Leu204Met)
c.133T>A (p.Leu45Met)
n.897T>A
11g.94476348C>ACA382376834MRE11c.600G>T (p.Met200Ile)
c.609G>T (p.Met203Ile)
c.132G>T (p.Met44Ile)
n.896G>T
11g.94476348C>GCA382376838MRE11c.600G>C (p.Met200Ile)
c.609G>C (p.Met203Ile)
c.132G>C (p.Met44Ile)
n.896G>C
11g.94476348C>TCA382376844MRE11c.600G>A (p.Met200Ile)
c.609G>A (p.Met203Ile)
c.132G>A (p.Met44Ile)
n.896G>A
11g.94476349A=CA1992433234MRE11c.599T= (p.Met200=)
c.608T= (p.Met203=)
c.131T= (p.Met44=)
n.895T=
11g.94476349A>CCA382376846MRE11c.599T>G (p.Met200Arg)
c.608T>G (p.Met203Arg)
c.131T>G (p.Met44Arg)
n.895T>G
11g.94476349A>GCA6235353MRE11c.599T>C (p.Met200Thr)
c.608T>C (p.Met203Thr)
c.131T>C (p.Met44Thr)
n.895T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476349A>TCA382376848MRE11c.599T>A (p.Met200Lys)
c.608T>A (p.Met203Lys)
c.131T>A (p.Met44Lys)
n.895T>A
11g.94476350T>ACA382376854MRE11c.598A>T (p.Met200Leu)
c.607A>T (p.Met203Leu)
c.130A>T (p.Met44Leu)
n.894A>T
11g.94476350T>CCA382376850MRE11c.598A>G (p.Met200Val)
c.607A>G (p.Met203Val)
c.130A>G (p.Met44Val)
n.894A>G
 ClinVar dbSNP
11g.94476350T>GCA382376853MRE11c.598A>C (p.Met200Leu)
c.607A>C (p.Met203Leu)
c.130A>C (p.Met44Leu)
n.894A>C
11g.94476350T=CA1992433243MRE11c.598A= (p.Met200=)
c.607A= (p.Met203=)
c.130A= (p.Met44=)
n.894A=
11g.94476351T>ACA476286764MRE11c.597A>T (p.Thr199=)
c.606A>T (p.Thr202=)
c.129A>T (p.Thr43=)
n.893A>T
 COSMIC
11g.94476351T>CCA476286765MRE11c.597A>G (p.Thr199=)
c.606A>G (p.Thr202=)
c.129A>G (p.Thr43=)
n.893A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.94476351T>GCA476286766MRE11c.597A>C (p.Thr199=)
c.606A>C (p.Thr202=)
c.129A>C (p.Thr43=)
n.893A>C
11g.94476351T=CA1992433247MRE11c.597A= (p.Thr199=)
c.606A= (p.Thr202=)
c.129A= (p.Thr43=)
n.893A=
11g.94476352G>ACA226532672MRE11c.596C>T (p.Thr199Ile)
c.605C>T (p.Thr202Ile)
c.128C>T (p.Thr43Ile)
n.892C>T
 ClinVar dbSNP gnomAD v4
11g.94476352G>CCA382376857MRE11c.596C>G (p.Thr199Arg)
c.605C>G (p.Thr202Arg)
c.128C>G (p.Thr43Arg)
n.892C>G
11g.94476352G=CA1992433254MRE11c.596C= (p.Thr199=)
c.605C= (p.Thr202=)
c.128C= (p.Thr43=)
n.892C=
11g.94476352G>TCA382376860MRE11c.596C>A (p.Thr199Lys)
c.605C>A (p.Thr202Lys)
c.128C>A (p.Thr43Lys)
n.892C>A
11g.94476353T>ACA382376864MRE11c.595A>T (p.Thr199Ser)
c.604A>T (p.Thr202Ser)
c.127A>T (p.Thr43Ser)
n.891A>T
11g.94476353T>CCA382376865MRE11c.595A>G (p.Thr199Ala)
c.604A>G (p.Thr202Ala)
c.127A>G (p.Thr43Ala)
n.891A>G
 gnomAD v4
11g.94476353T>GCA382376866MRE11c.595A>C (p.Thr199Pro)
c.604A>C (p.Thr202Pro)
c.127A>C (p.Thr43Pro)
n.891A>C
11g.94476354T>ACA476286769MRE11c.594A>T (p.Val198=)
c.603A>T (p.Val201=)
c.126A>T (p.Val42=)
n.890A>T
11g.94476354T>CCA476286770MRE11c.594A>G (p.Val198=)
c.603A>G (p.Val201=)
c.126A>G (p.Val42=)
n.890A>G
11g.94476354T>GCA476286768MRE11c.594A>C (p.Val198=)
c.603A>C (p.Val201=)
c.126A>C (p.Val42=)
n.890A>C
11g.94476355A>CCA382376868MRE11c.593T>G (p.Val198Gly)
c.602T>G (p.Val201Gly)
c.125T>G (p.Val42Gly)
n.889T>G
 ClinVar gnomAD v4
11g.94476355A>GCA382376869MRE11c.593T>C (p.Val198Ala)
c.602T>C (p.Val201Ala)
c.125T>C (p.Val42Ala)
n.889T>C
 gnomAD v4
11g.94476355A>TCA382376872MRE11c.593T>A (p.Val198Glu)
c.602T>A (p.Val201Glu)
c.125T>A (p.Val42Glu)
n.889T>A
11g.94476355_94476356delinsACCA1992433260MRE11c.592_593delinsGT (p.Val198=)
c.601_602delinsGT (p.Val201=)
c.124_125delinsGT (p.Val42=)
n.888_889delinsGT
11g.94476356delCA600841621MRE11c.592del (p.Val198Ter)
c.601del (p.Val201Ter)
c.124del (p.Val42Ter)
n.888del
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.94476356C>ACA10579405MRE11c.592G>T (p.Val198Leu)
c.601G>T (p.Val201Leu)
c.124G>T (p.Val42Leu)
n.888G>T
 ClinVar dbSNP
11g.94476356C=CA1992433263MRE11c.592G= (p.Val198=)
c.601G= (p.Val201=)
c.124G= (p.Val42=)
n.888G=
11g.94476356C>GCA382376875MRE11c.592G>C (p.Val198Leu)
c.601G>C (p.Val201Leu)
c.124G>C (p.Val42Leu)
n.888G>C
11g.94476356C>TCA382376876MRE11c.592G>A (p.Val198Ile)
c.601G>A (p.Val201Ile)
c.124G>A (p.Val42Ile)
n.888G>A
11g.94476357T>ACA382376878MRE11c.591A>T (p.Lys197Asn)
c.600A>T (p.Lys200Asn)
c.123A>T (p.Lys41Asn)
n.887A>T
11g.94476357T>CCA476286774MRE11c.591A>G (p.Lys197=)
c.600A>G (p.Lys200=)
c.123A>G (p.Lys41=)
n.887A>G
11g.94476357T>GCA382376880MRE11c.591A>C (p.Lys197Asn)
c.600A>C (p.Lys200Asn)
c.123A>C (p.Lys41Asn)
n.887A>C
11g.94476362dupCA2615589633MRE11c.591dup (p.Val198SerfsTer10)
c.600dup (p.Val201SerfsTer10)
c.123dup (p.Val42SerfsTer10)
n.887dup
 gnomAD v4
11g.94476362delCA2615589634MRE11c.591del (p.Val198Ter)
c.600del (p.Val201Ter)
c.123del (p.Val42Ter)
n.887del
 dbSNP gnomAD v4
11g.94476358T>ACA382376881MRE11c.590A>T (p.Lys197Ile)
c.599A>T (p.Lys200Ile)
c.122A>T (p.Lys41Ile)
n.886A>T
11g.94476358T>CCA382376883MRE11c.590A>G (p.Lys197Arg)
c.599A>G (p.Lys200Arg)
c.122A>G (p.Lys41Arg)
n.886A>G
11g.94476358T>GCA382376885MRE11c.590A>C (p.Lys197Thr)
c.599A>C (p.Lys200Thr)
c.122A>C (p.Lys41Thr)
n.886A>C
11g.94476359T>ACA382376887MRE11c.589A>T (p.Lys197Ter)
c.598A>T (p.Lys200Ter)
c.121A>T (p.Lys41Ter)
n.885A>T
11g.94476359T>CCA382376889MRE11c.589A>G (p.Lys197Glu)
c.598A>G (p.Lys200Glu)
c.121A>G (p.Lys41Glu)
n.885A>G
11g.94476359T>GCA382376890MRE11c.589A>C (p.Lys197Gln)
c.598A>C (p.Lys200Gln)
c.121A>C (p.Lys41Gln)
n.885A>C
11g.94476360T>ACA382376892MRE11c.588A>T (p.Lys196Asn)
c.597A>T (p.Lys199Asn)
c.120A>T (p.Lys40Asn)
n.884A>T
11g.94476360T>CCA195920MRE11c.588A>G (p.Lys196=)
c.597A>G (p.Lys199=)
c.120A>G (p.Lys40=)
n.884A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.94476360T>GCA382376894MRE11c.588A>C (p.Lys196Asn)
c.597A>C (p.Lys199Asn)
c.120A>C (p.Lys40Asn)
n.884A>C
11g.94476360T=CA1992433268MRE11c.588A= (p.Lys196=)
c.597A= (p.Lys199=)
c.120A= (p.Lys40=)
n.884A=
11g.94476361T>ACA382376895MRE11c.587A>T (p.Lys196Ile)
c.596A>T (p.Lys199Ile)
c.119A>T (p.Lys40Ile)
n.883A>T
11g.94476361T>CCA6235354MRE11c.587A>G (p.Lys196Arg)
c.596A>G (p.Lys199Arg)
c.119A>G (p.Lys40Arg)
n.883A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.94476361T>GCA382376897MRE11c.587A>C (p.Lys196Thr)
c.596A>C (p.Lys199Thr)
c.119A>C (p.Lys40Thr)
n.883A>C
11g.94476361T=CA1992433271MRE11c.587A= (p.Lys196=)
c.596A= (p.Lys199=)
c.119A= (p.Lys40=)
n.883A=
11g.94476363_94476365delCA2615589635MRE11c.585_587del (p.Asn195del)
c.594_596del (p.Asn198del)
c.117_119del (p.Asn39del)
n.881_883del
 gnomAD v4
11g.94476362T>ACA382376902MRE11c.586A>T (p.Lys196Ter)
c.595A>T (p.Lys199Ter)
c.118A>T (p.Lys40Ter)
n.882A>T
11g.94476362T>CCA382376901MRE11c.586A>G (p.Lys196Glu)
c.595A>G (p.Lys199Glu)
c.118A>G (p.Lys40Glu)
n.882A>G
 ClinVar dbSNP
11g.94476362T>GCA382376899MRE11c.586A>C (p.Lys196Gln)
c.595A>C (p.Lys199Gln)
c.118A>C (p.Lys40Gln)
n.882A>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.94476362T=CA1992433275MRE11c.586A= (p.Lys196=)
c.595A= (p.Lys199=)
c.118A= (p.Lys40=)
n.882A=
11g.94476363A=CA1992433279MRE11c.585T= (p.Asn195=)
c.594T= (p.Asn198=)
c.117T= (p.Asn39=)
n.881T=
11g.94476363A>CCA382376905MRE11c.585T>G (p.Asn195Lys)
c.594T>G (p.Asn198Lys)
c.117T>G (p.Asn39Lys)
n.881T>G
11g.94476363A>GCA10635935MRE11c.585T>C (p.Asn195=)
c.594T>C (p.Asn198=)
c.117T>C (p.Asn39=)
n.881T>C
 ClinVar dbSNP COSMIC COSMIC
11g.94476363A>TCA382376907MRE11c.585T>A (p.Asn195Lys)
c.594T>A (p.Asn198Lys)
c.117T>A (p.Asn39Lys)
n.881T>A
11g.94476364T>ACA382376909MRE11c.584A>T (p.Asn195Ile)
c.593A>T (p.Asn198Ile)
c.116A>T (p.Asn39Ile)
n.880A>T
11g.94476364T>CCA382376910MRE11c.584A>G (p.Asn195Ser)
c.593A>G (p.Asn198Ser)
c.116A>G (p.Asn39Ser)
n.880A>G
 ClinVar dbSNP
11g.94476364T>GCA382376912MRE11c.584A>C (p.Asn195Thr)
c.593A>C (p.Asn198Thr)
c.116A>C (p.Asn39Thr)
n.880A>C
11g.94476364T=CA1992433289MRE11c.584A= (p.Asn195=)
c.593A= (p.Asn198=)
c.116A= (p.Asn39=)
n.880A=
11g.94476365T>ACA382376914MRE11c.583A>T (p.Asn195Tyr)
c.592A>T (p.Asn198Tyr)
c.115A>T (p.Asn39Tyr)
n.879A>T
11g.94476365T>CCA382376916MRE11c.583A>G (p.Asn195Asp)
c.592A>G (p.Asn198Asp)
c.115A>G (p.Asn39Asp)
n.879A>G
11g.94476365T>GCA382376918MRE11c.583A>C (p.Asn195His)
c.592A>C (p.Asn198His)
c.115A>C (p.Asn39His)
n.879A>C
11g.94476366G>ACA476286777MRE11c.582C>T (p.Val194=)
c.591C>T (p.Val197=)
c.114C>T (p.Val38=)
n.878C>T
 ClinVar dbSNP gnomAD v4
11g.94476366G>CCA476286778MRE11c.582C>G (p.Val194=)
c.591C>G (p.Val197=)
c.114C>G (p.Val38=)
n.878C>G
 ClinVar
11g.94476366G=CA1992433291MRE11c.582C= (p.Val194=)
c.591C= (p.Val197=)
c.114C= (p.Val38=)
n.878C=
11g.94476366G>TCA476286779MRE11c.582C>A (p.Val194=)
c.591C>A (p.Val197=)
c.114C>A (p.Val38=)
n.878C>A
 dbSNP
11g.94476367A=CA1992433297MRE11c.581T= (p.Val194=)
c.590T= (p.Val197=)
c.113T= (p.Val38=)
n.877T=
11g.94476367A>CCA382376919MRE11c.581T>G (p.Val194Gly)
c.590T>G (p.Val197Gly)
c.113T>G (p.Val38Gly)
n.877T>G
 gnomAD v4
11g.94476367A>GCA382376921MRE11c.581T>C (p.Val194Ala)
c.590T>C (p.Val197Ala)
c.113T>C (p.Val38Ala)
n.877T>C
 ClinVar dbSNP
11g.94476367A>TCA382376922MRE11c.581T>A (p.Val194Asp)
c.590T>A (p.Val197Asp)
c.113T>A (p.Val38Asp)
n.877T>A
11g.94476367_94476368insAATGCCCTTAATCTTTCA918943633MRE11c.580_581insAAAGATTAAGGGCATT (p.Val194GlufsTer8)
c.589_590insAAAGATTAAGGGCATT (p.Val197GlufsTer8)
c.112_113insAAAGATTAAGGGCATT (p.Val38GlufsTer8)
n.876_877insAAAGATTAAGGGCATT
 dbSNP
11g.94476368C>ACA382376927MRE11c.580G>T (p.Val194Phe)
c.589G>T (p.Val197Phe)
c.112G>T (p.Val38Phe)
n.876G>T
 dbSNP gnomAD v2 gnomAD v4
11g.94476368C=CA1992433301MRE11c.580G= (p.Val194=)
c.589G= (p.Val197=)
c.112G= (p.Val38=)
n.876G=
11g.94476368C>GCA382376925MRE11c.580G>C (p.Val194Leu)
c.589G>C (p.Val197Leu)
c.112G>C (p.Val38Leu)
n.876G>C
11g.94476368C>TCA382376924MRE11c.580G>A (p.Val194Ile)
c.589G>A (p.Val197Ile)
c.112G>A (p.Val38Ile)
n.876G>A
11g.94476369A=CA1992433310MRE11c.579T= (p.Phe193=)
c.588T= (p.Phe196=)
c.111T= (p.Phe37=)
n.875T=
11g.94476369A>CCA382376929MRE11c.579T>G (p.Phe193Leu)
c.588T>G (p.Phe196Leu)
c.111T>G (p.Phe37Leu)
n.875T>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.94476369A>GCA476286780MRE11c.579T>C (p.Phe193=)
c.588T>C (p.Phe196=)
c.111T>C (p.Phe37=)
n.875T>C
11g.94476369A>TCA382376930MRE11c.579T>A (p.Phe193Leu)
c.588T>A (p.Phe196Leu)
c.111T>A (p.Phe37Leu)
n.875T>A
11g.94476370A>CCA382376932MRE11c.578T>G (p.Phe193Cys)
c.587T>G (p.Phe196Cys)
c.110T>G (p.Phe37Cys)
n.874T>G
11g.94476370A>GCA382376935MRE11c.578T>C (p.Phe193Ser)
c.587T>C (p.Phe196Ser)
c.110T>C (p.Phe37Ser)
n.874T>C
11g.94476370A>TCA382376933MRE11c.578T>A (p.Phe193Tyr)
c.587T>A (p.Phe196Tyr)
c.110T>A (p.Phe37Tyr)
n.874T>A
11g.94476370_94476371insGGTTGTCCA2724798586MRE11c.577_578insGACAACC (p.Phe193Ter)
c.586_587insGACAACC (p.Phe196Ter)
c.109_110insGACAACC (p.Phe37Ter)
n.873_874insGACAACC
 dbSNP
11g.94476371A>CCA382376937MRE11c.577T>G (p.Phe193Val)
c.586T>G (p.Phe196Val)
c.109T>G (p.Phe37Val)
n.873T>G
11g.94476371A>GCA382376939MRE11c.577T>C (p.Phe193Leu)
c.586T>C (p.Phe196Leu)
c.109T>C (p.Phe37Leu)
n.873T>C
11g.94476371A>TCA382376940MRE11c.577T>A (p.Phe193Ile)
c.586T>A (p.Phe196Ile)
c.109T>A (p.Phe37Ile)
n.873T>A
 gnomAD v4
11g.94476371_94476372insGTGCAAGATCA2724798611MRE11c.576_577insATCTTGCAC (p.Met192_Phe193insIleLeuHis)
c.585_586insATCTTGCAC (p.Met195_Phe196insIleLeuHis)
c.108_109insATCTTGCAC (p.Met36_Phe37insIleLeuHis)
n.872_873insATCTTGCAC
 dbSNP
11g.94476372C>ACA382376942MRE11c.576G>T (p.Met192Ile)
c.585G>T (p.Met195Ile)
c.108G>T (p.Met36Ile)
n.872G>T
11g.94476372C=CA1992433315MRE11c.576G= (p.Met192=)
c.585G= (p.Met195=)
c.108G= (p.Met36=)
n.872G=
11g.94476372C>GCA382376944MRE11c.576G>C (p.Met192Ile)
c.585G>C (p.Met195Ile)
c.108G>C (p.Met36Ile)
n.872G>C
 ClinVar gnomAD v4
11g.94476372C>TCA382376946MRE11c.576G>A (p.Met192Ile)
c.585G>A (p.Met195Ile)
c.108G>A (p.Met36Ile)
n.872G>A
 ClinVar dbSNP gnomAD v4
11g.94476373A>CCA382376948MRE11c.575T>G (p.Met192Arg)
c.584T>G (p.Met195Arg)
c.107T>G (p.Met36Arg)
n.871T>G
11g.94476373A>GCA382376949MRE11c.575T>C (p.Met192Thr)
c.584T>C (p.Met195Thr)
c.107T>C (p.Met36Thr)
n.871T>C
11g.94476373A>TCA382376951MRE11c.575T>A (p.Met192Lys)
c.584T>A (p.Met195Lys)
c.107T>A (p.Met36Lys)
n.871T>A
11g.94476374T>ACA382376953MRE11c.574A>T (p.Met192Leu)
c.583A>T (p.Met195Leu)
c.106A>T (p.Met36Leu)
n.870A>T
11g.94476374T>CCA382376955MRE11c.574A>G (p.Met192Val)
c.583A>G (p.Met195Val)
c.106A>G (p.Met36Val)
n.870A>G
11g.94476374T>GCA382376956MRE11c.574A>C (p.Met192Leu)
c.583A>C (p.Met195Leu)
c.106A>C (p.Met36Leu)
n.870A>C
11g.94476375T>ACA476286782MRE11c.573A>T (p.Arg191=)
c.582A>T (p.Arg194=)
c.105A>T (p.Arg35=)
n.869A>T
11g.94476375T>CCA476286784MRE11c.573A>G (p.Arg191=)
c.582A>G (p.Arg194=)
c.105A>G (p.Arg35=)
n.869A>G
11g.94476375T>GCA476286783MRE11c.573A>C (p.Arg191=)
c.582A>C (p.Arg194=)
c.105A>C (p.Arg35=)
n.869A>C
 ClinVar dbSNP gnomAD v4
11g.94476375T=CA1992433320MRE11c.573A= (p.Arg191=)
c.582A= (p.Arg194=)
c.105A= (p.Arg35=)
n.869A=
11g.94476376C>ACA382376961MRE11c.572G>T (p.Arg191Leu)
c.581G>T (p.Arg194Leu)
c.104G>T (p.Arg35Leu)
n.868G>T
 ClinVar dbSNP
11g.94476376C=CA1992433332MRE11c.572G= (p.Arg191=)
c.581G= (p.Arg194=)
c.104G= (p.Arg35=)
n.868G=
11g.94476376C>GCA382376958MRE11c.572G>C (p.Arg191Pro)
c.581G>C (p.Arg194Pro)
c.104G>C (p.Arg35Pro)
n.868G>C
11g.94476376C>TCA6235355MRE11c.572G>A (p.Arg191Gln)
c.581G>A (p.Arg194Gln)
c.104G>A (p.Arg35Gln)
n.868G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476377G>ACA382376962MRE11c.571C>T (p.Arg191Ter)
c.580C>T (p.Arg194Ter)
c.103C>T (p.Arg35Ter)
n.867C>T
 ClinVar dbSNP gnomAD v4
11g.94476377G>CCA382376964MRE11c.571C>G (p.Arg191Gly)
c.580C>G (p.Arg194Gly)
c.103C>G (p.Arg35Gly)
n.867C>G
 ClinVar gnomAD v4
11g.94476377G=CA1992433342MRE11c.571C= (p.Arg191=)
c.580C= (p.Arg194=)
c.103C= (p.Arg35=)
n.867C=
11g.94476377G>TCA476286785MRE11c.571C>A (p.Arg191=)
c.580C>A (p.Arg194=)
c.103C>A (p.Arg35=)
n.867C>A
 ClinVar gnomAD v4
11g.94476378A>CCA382376966MRE11c.570T>G (p.Tyr190Ter)
c.579T>G (p.Tyr193Ter)
c.102T>G (p.Tyr34Ter)
n.866T>G
11g.94476378A>GCA476286786MRE11c.570T>C (p.Tyr190=)
c.579T>C (p.Tyr193=)
c.102T>C (p.Tyr34=)
n.866T>C
 ClinVar
11g.94476378A>TCA382376968MRE11c.570T>A (p.Tyr190Ter)
c.579T>A (p.Tyr193Ter)
c.102T>A (p.Tyr34Ter)
n.866T>A
11g.94476379T>ACA382376969MRE11c.569A>T (p.Tyr190Phe)
c.578A>T (p.Tyr193Phe)
c.101A>T (p.Tyr34Phe)
n.865A>T
11g.94476379T>CCA226532683MRE11c.569A>G (p.Tyr190Cys)
c.578A>G (p.Tyr193Cys)
c.101A>G (p.Tyr34Cys)
n.865A>G
 ClinVar dbSNP gnomAD v4
11g.94476379T>GCA382376970MRE11c.569A>C (p.Tyr190Ser)
c.578A>C (p.Tyr193Ser)
c.101A>C (p.Tyr34Ser)
n.865A>C
11g.94476379T=CA1992433344MRE11c.569A= (p.Tyr190=)
c.578A= (p.Tyr193=)
c.101A= (p.Tyr34=)
n.865A=
11g.94476380A>CCA382376971MRE11c.568T>G (p.Tyr190Asp)
c.577T>G (p.Tyr193Asp)
c.100T>G (p.Tyr34Asp)
n.864T>G
11g.94476380A>GCA382376973MRE11c.568T>C (p.Tyr190His)
c.577T>C (p.Tyr193His)
c.100T>C (p.Tyr34His)
n.864T>C
 COSMIC
11g.94476380A>TCA382376975MRE11c.568T>A (p.Tyr190Asn)
c.577T>A (p.Tyr193Asn)
c.100T>A (p.Tyr34Asn)
n.864T>A
11g.94476381G>ACA476286787MRE11c.567C>T (p.Leu189=)
c.576C>T (p.Leu192=)
c.99C>T (p.Leu33=)
n.863C>T
 gnomAD v4
11g.94476381G>CCA476286788MRE11c.567C>G (p.Leu189=)
c.576C>G (p.Leu192=)
c.99C>G (p.Leu33=)
n.863C>G
 ClinVar dbSNP
11g.94476381G>TCA476286789MRE11c.567C>A (p.Leu189=)
c.576C>A (p.Leu192=)
c.99C>A (p.Leu33=)
n.863C>A
 gnomAD v4
11g.94476382A>CCA382376978MRE11c.566T>G (p.Leu189Arg)
c.575T>G (p.Leu192Arg)
c.98T>G (p.Leu33Arg)
n.862T>G
11g.94476382A>GCA382376977MRE11c.566T>C (p.Leu189Pro)
c.575T>C (p.Leu192Pro)
c.98T>C (p.Leu33Pro)
n.862T>C
11g.94476382A>TCA382376976MRE11c.566T>A (p.Leu189His)
c.575T>A (p.Leu192His)
c.98T>A (p.Leu33His)
n.862T>A
11g.94476383G>ACA382376981MRE11c.565C>T (p.Leu189Phe)
c.574C>T (p.Leu192Phe)
c.97C>T (p.Leu33Phe)
n.861C>T
 ClinVar dbSNP gnomAD v4
11g.94476383G>CCA382376982MRE11c.565C>G (p.Leu189Val)
c.574C>G (p.Leu192Val)
c.97C>G (p.Leu33Val)
n.861C>G
11g.94476383G=CA1992433350MRE11c.565C= (p.Leu189=)
c.574C= (p.Leu192=)
c.97C= (p.Leu33=)
n.861C=
11g.94476383G>TCA382376983MRE11c.565C>A (p.Leu189Ile)
c.574C>A (p.Leu192Ile)
c.97C>A (p.Leu33Ile)
n.861C>A
 gnomAD v4
11g.94476384C>ACA6235357MRE11c.564G>T (p.Arg188Ser)
c.573G>T (p.Arg191Ser)
c.96G>T (p.Arg32Ser)
n.860G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476384C=CA1992433358MRE11c.564G= (p.Arg188=)
c.573G= (p.Arg191=)
c.96G= (p.Arg32=)
n.860G=
11g.94476384C>GCA10579406MRE11c.564G>C (p.Arg188Ser)
c.573G>C (p.Arg191Ser)
c.96G>C (p.Arg32Ser)
n.860G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.94476384C>TCA6235356MRE11c.564G>A (p.Arg188=)
c.573G>A (p.Arg191=)
c.96G>A (p.Arg32=)
n.860G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.94476385C>ACA382376987MRE11c.563G>T (p.Arg188Met)
c.572G>T (p.Arg191Met)
c.95G>T (p.Arg32Met)
n.859G>T
11g.94476385C=CA1992433365MRE11c.563G= (p.Arg188=)
c.572G= (p.Arg191=)
c.95G= (p.Arg32=)
n.859G=
11g.94476385C>GCA382376989MRE11c.563G>C (p.Arg188Thr)
c.572G>C (p.Arg191Thr)
c.95G>C (p.Arg32Thr)
n.859G>C
11g.94476385C>TCA382376991MRE11c.563G>A (p.Arg188Lys)
c.572G>A (p.Arg191Lys)
c.95G>A (p.Arg32Lys)
n.859G>A
 ClinVar dbSNP
11g.94476386T>ACA382376993MRE11c.562A>T (p.Arg188Trp)
c.571A>T (p.Arg191Trp)
c.94A>T (p.Arg32Trp)
n.858A>T
11g.94476386T>CCA382376995MRE11c.562A>G (p.Arg188Gly)
c.571A>G (p.Arg191Gly)
c.94A>G (p.Arg32Gly)
n.858A>G
 ClinVar dbSNP
11g.94476386T>GCA476286790MRE11c.562A>C (p.Arg188=)
c.571A>C (p.Arg191=)
c.94A>C (p.Arg32=)
n.858A>C
 ClinVar
11g.94476386T=CA1992433367MRE11c.562A= (p.Arg188=)
c.571A= (p.Arg191=)
c.94A= (p.Arg32=)
n.858A=
11g.94476387T>ACA382376997MRE11c.561A>T (p.Glu187Asp)
c.570A>T (p.Glu190Asp)
c.93A>T (p.Glu31Asp)
n.857A>T
11g.94476387T>CCA476286791MRE11c.561A>G (p.Glu187=)
c.570A>G (p.Glu190=)
c.93A>G (p.Glu31=)
n.857A>G
 ClinVar dbSNP
11g.94476387T>GCA382376998MRE11c.561A>C (p.Glu187Asp)
c.570A>C (p.Glu190Asp)
c.93A>C (p.Glu31Asp)
n.857A>C
 gnomAD v4
11g.94476388T>ACA382377000MRE11c.560A>T (p.Glu187Val)
c.569A>T (p.Glu190Val)
c.92A>T (p.Glu31Val)
n.856A>T
11g.94476388T>CCA382377003MRE11c.560A>G (p.Glu187Gly)
c.569A>G (p.Glu190Gly)
c.92A>G (p.Glu31Gly)
n.856A>G
11g.94476388T>GCA382377002MRE11c.560A>C (p.Glu187Ala)
c.569A>C (p.Glu190Ala)
c.92A>C (p.Glu31Ala)
n.856A>C
11g.94476389C>ACA382377004MRE11c.559G>T (p.Glu187Ter)
c.568G>T (p.Glu190Ter)
c.91G>T (p.Glu31Ter)
n.855G>T
11g.94476389C=CA1992433371MRE11c.559G= (p.Glu187=)
c.568G= (p.Glu190=)
c.91G= (p.Glu31=)
n.855G=
11g.94476389C>GCA382377005MRE11c.559G>C (p.Glu187Gln)
c.568G>C (p.Glu190Gln)
c.91G>C (p.Glu31Gln)
n.855G>C
11g.94476389C>TCA6235358MRE11c.559G>A (p.Glu187Lys)
c.568G>A (p.Glu190Lys)
c.91G>A (p.Glu31Lys)
n.855G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476390A=CA1992433375MRE11c.558T= (p.Asp186=)
c.567T= (p.Asp189=)
c.90T= (p.Asp30=)
n.854T=
11g.94476390A>CCA382377009MRE11c.558T>G (p.Asp186Glu)
c.567T>G (p.Asp189Glu)
c.90T>G (p.Asp30Glu)
n.854T>G
11g.94476390A>GCA476286792MRE11c.558T>C (p.Asp186=)
c.567T>C (p.Asp189=)
c.90T>C (p.Asp30=)
n.854T>C
 ClinVar dbSNP gnomAD v4
11g.94476390A>TCA382377010MRE11c.558T>A (p.Asp186Glu)
c.567T>A (p.Asp189Glu)
c.90T>A (p.Asp30Glu)
n.854T>A
 gnomAD v4
11g.94476391T>ACA382377011MRE11c.557A>T (p.Asp186Val)
c.566A>T (p.Asp189Val)
c.89A>T (p.Asp30Val)
n.853A>T
11g.94476391T>CCA382377012MRE11c.557A>G (p.Asp186Gly)
c.566A>G (p.Asp189Gly)
c.89A>G (p.Asp30Gly)
n.853A>G
11g.94476391T>GCA382377013MRE11c.557A>C (p.Asp186Ala)
c.566A>C (p.Asp189Ala)
c.89A>C (p.Asp30Ala)
n.853A>C
11g.94476392C>ACA382377014MRE11c.556G>T (p.Asp186Tyr)
c.565G>T (p.Asp189Tyr)
c.88G>T (p.Asp30Tyr)
n.852G>T
 ClinVar dbSNP gnomAD v2
11g.94476392C=CA1992433379MRE11c.556G= (p.Asp186=)
c.565G= (p.Asp189=)
c.88G= (p.Asp30=)
n.852G=
11g.94476392C>GCA382377015MRE11c.556G>C (p.Asp186His)
c.565G>C (p.Asp189His)
c.88G>C (p.Asp30His)
n.852G>C
11g.94476392C>TCA382377016MRE11c.556G>A (p.Asp186Asn)
c.565G>A (p.Asp189Asn)
c.88G>A (p.Asp30Asn)
n.852G>A
 dbSNP
11g.94476393T>ACA476286793MRE11c.555A>T (p.Pro185=)
c.564A>T (p.Pro188=)
c.87A>T (p.Pro29=)
n.851A>T
11g.94476393T>CCA476286794MRE11c.555A>G (p.Pro185=)
c.564A>G (p.Pro188=)
c.87A>G (p.Pro29=)
n.851A>G
11g.94476393T>GCA476286795MRE11c.555A>C (p.Pro185=)
c.564A>C (p.Pro188=)
c.87A>C (p.Pro29=)
n.851A>C
11g.94476394G>ACA382377019MRE11c.554C>T (p.Pro185Leu)
c.563C>T (p.Pro188Leu)
c.86C>T (p.Pro29Leu)
n.850C>T
11g.94476394G>CCA382377020MRE11c.554C>G (p.Pro185Arg)
c.563C>G (p.Pro188Arg)
c.86C>G (p.Pro29Arg)
n.850C>G
11g.94476394G>TCA382377017MRE11c.554C>A (p.Pro185Gln)
c.563C>A (p.Pro188Gln)
c.86C>A (p.Pro29Gln)
n.850C>A
11g.94476395G>ACA382377023MRE11c.553C>T (p.Pro185Ser)
c.562C>T (p.Pro188Ser)
c.85C>T (p.Pro29Ser)
n.849C>T
 gnomAD v4
11g.94476395G>CCA169851MRE11c.553C>G (p.Pro185Ala)
c.562C>G (p.Pro188Ala)
c.85C>G (p.Pro29Ala)
n.849C>G
 ClinVar dbSNP
11g.94476395G=CA1992433383MRE11c.553C= (p.Pro185=)
c.562C= (p.Pro188=)
c.85C= (p.Pro29=)
n.849C=
11g.94476395G>TCA382377022MRE11c.553C>A (p.Pro185Thr)
c.562C>A (p.Pro188Thr)
c.85C>A (p.Pro29Thr)
n.849C>A
11g.94476395_94476396delinsGACA1992433389MRE11c.552_553delinsTC (p.Ile184=)
c.561_562delinsTC (p.Ile187=)
c.84_85delinsTC (p.Ile28=)
n.848_849delinsTC
11g.94476396A>CCA382377025MRE11c.552T>G (p.Ile184Met)
c.561T>G (p.Ile187Met)
c.84T>G (p.Ile28Met)
n.848T>G
11g.94476396A>GCA476286798MRE11c.552T>C (p.Ile184=)
c.561T>C (p.Ile187=)
c.84T>C (p.Ile28=)
n.848T>C
11g.94476396A>TCA476286797MRE11c.552T>A (p.Ile184=)
c.561T>A (p.Ile187=)
c.84T>A (p.Ile28=)
n.848T>A
11g.94476397delCA1139662136MRE11c.552del (p.Pro185GlnfsTer14)
c.561del (p.Pro188GlnfsTer14)
c.84del (p.Pro29GlnfsTer14)
n.848del
 ClinVar dbSNP
11g.94476397A>CCA382377026MRE11c.551T>G (p.Ile184Ser)
c.560T>G (p.Ile187Ser)
c.83T>G (p.Ile28Ser)
n.847T>G
11g.94476397A>GCA382377027MRE11c.551T>C (p.Ile184Thr)
c.560T>C (p.Ile187Thr)
c.83T>C (p.Ile28Thr)
n.847T>C
 gnomAD v4
11g.94476397A>TCA382377028MRE11c.551T>A (p.Ile184Asn)
c.560T>A (p.Ile187Asn)
c.83T>A (p.Ile28Asn)
n.847T>A
11g.94476398T>ACA382377030MRE11c.550A>T (p.Ile184Phe)
c.559A>T (p.Ile187Phe)
c.82A>T (p.Ile28Phe)
n.846A>T
11g.94476398T>CCA382377031MRE11c.550A>G (p.Ile184Val)
c.559A>G (p.Ile187Val)
c.82A>G (p.Ile28Val)
n.846A>G
 gnomAD v4
11g.94476398T>GCA382377033MRE11c.550A>C (p.Ile184Leu)
c.559A>C (p.Ile187Leu)
c.82A>C (p.Ile28Leu)
n.846A>C
 gnomAD v4
11g.94476399G>ACA476286799MRE11c.549C>T (p.Ser183=)
c.558C>T (p.Ser186=)
c.81C>T (p.Ser27=)
n.845C>T
 ClinVar
11g.94476399G>CCA476286800MRE11c.549C>G (p.Ser183=)
c.558C>G (p.Ser186=)
c.81C>G (p.Ser27=)
n.845C>G
11g.94476399G>TCA476286801MRE11c.549C>A (p.Ser183=)
c.558C>A (p.Ser186=)
c.81C>A (p.Ser27=)
n.845C>A
 gnomAD v4
11g.94476400G>ACA382377034MRE11c.548C>T (p.Ser183Phe)
c.557C>T (p.Ser186Phe)
c.80C>T (p.Ser27Phe)
n.844C>T
11g.94476400G>CCA382377036MRE11c.548C>G (p.Ser183Cys)
c.557C>G (p.Ser186Cys)
c.80C>G (p.Ser27Cys)
n.844C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.94476400G=CA1992433400MRE11c.548C= (p.Ser183=)
c.557C= (p.Ser186=)
c.80C= (p.Ser27=)
n.844C=
11g.94476400G>TCA382377038MRE11c.548C>A (p.Ser183Tyr)
c.557C>A (p.Ser186Tyr)
c.80C>A (p.Ser27Tyr)
n.844C>A
 gnomAD v4
11g.94476401A>CCA382377042MRE11c.547T>G (p.Ser183Ala)
c.556T>G (p.Ser186Ala)
c.79T>G (p.Ser27Ala)
n.843T>G
11g.94476401A>GCA382377044MRE11c.547T>C (p.Ser183Pro)
c.556T>C (p.Ser186Pro)
c.79T>C (p.Ser27Pro)
n.843T>C
11g.94476401A>TCA382377040MRE11c.547T>A (p.Ser183Thr)
c.556T>A (p.Ser186Thr)
c.79T>A (p.Ser27Thr)
n.843T>A
11g.94476402T>ACA476286802MRE11c.546A>T (p.Gly182=)
c.555A>T (p.Gly185=)
c.78A>T (p.Gly26=)
n.842A>T
 dbSNP gnomAD v2 gnomAD v4
11g.94476402T>CCA476286803MRE11c.546A>G (p.Gly182=)
c.555A>G (p.Gly185=)
c.78A>G (p.Gly26=)
n.842A>G
 gnomAD v4
11g.94476402T>GCA476286804MRE11c.546A>C (p.Gly182=)
c.555A>C (p.Gly185=)
c.78A>C (p.Gly26=)
n.842A>C
11g.94476402T=CA1992433405MRE11c.546A= (p.Gly182=)
c.555A= (p.Gly185=)
c.78A= (p.Gly26=)
n.842A=
11g.94476403C>ACA382377045MRE11c.545G>T (p.Gly182Val)
c.554G>T (p.Gly185Val)
c.77G>T (p.Gly26Val)
n.841G>T
 dbSNP gnomAD v4
11g.94476403C>GCA382377047MRE11c.545G>C (p.Gly182Ala)
c.554G>C (p.Gly185Ala)
c.77G>C (p.Gly26Ala)
n.841G>C
11g.94476403C>TCA382377048MRE11c.545G>A (p.Gly182Glu)
c.554G>A (p.Gly185Glu)
c.77G>A (p.Gly26Glu)
n.841G>A
 ClinVar
11g.94476404C>ACA382377049MRE11c.545-1G>T (n.545-1G>T)
c.554-1G>T (n.554-1G>T)
c.77-1G>T (n.77-1G>T)
n.841-1G>T
11g.94476404C=CA1992433415MRE11c.545-1G= (n.545-1G=)
c.554-1G= (n.554-1G=)
c.77-1G= (n.77-1G=)
n.841-1G=
11g.94476404C>GCA382377050MRE11c.545-1G>C (n.545-1G>C)
c.554-1G>C (n.554-1G>C)
c.77-1G>C (n.77-1G>C)
n.841-1G>C
11g.94476404C>TCA382377052MRE11c.545-1G>A (n.545-1G>A)
c.554-1G>A (n.554-1G>A)
c.77-1G>A (n.77-1G>A)
n.841-1G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.94476405T>ACA382377053MRE11c.545-2A>T (n.545-2A>T)
c.554-2A>T (n.554-2A>T)
c.77-2A>T (n.77-2A>T)
n.841-2A>T
11g.94476405T>CCA382377055MRE11c.545-2A>G (n.545-2A>G)
c.554-2A>G (n.554-2A>G)
c.77-2A>G (n.77-2A>G)
n.841-2A>G
 gnomAD v4
11g.94476405T>GCA382377054MRE11c.545-2A>C (n.545-2A>C)
c.554-2A>C (n.554-2A>C)
c.77-2A>C (n.77-2A>C)
n.841-2A>C
11g.94476406G>ACA658658086MRE11c.545-3C>T (n.545-3C>T)
c.554-3C>T (n.554-3C>T)
c.77-3C>T (n.77-3C>T)
n.841-3C>T
 ClinVar dbSNP gnomAD v4
11g.94476406G=CA1992433423MRE11c.545-3C= (n.545-3C=)
c.554-3C= (n.554-3C=)
c.77-3C= (n.77-3C=)
n.841-3C=
11g.94476406G>TCA2615589702MRE11c.545-3C>A (n.545-3C>A)
c.554-3C>A (n.554-3C>A)
c.77-3C>A (n.77-3C>A)
n.841-3C>A
 gnomAD v4
11g.94476409delCA2615589704MRE11c.545-4del (n.545-4del)
c.554-4del (n.554-4del)
c.77-4del (n.77-4del)
n.841-4del
 gnomAD v4
11g.94476410T>CCA2793218205MRE11c.545-7A>G (n.545-7A>G)
c.554-7A>G (n.554-7A>G)
c.77-7A>G (n.77-7A>G)
n.841-7A>G
11g.94476410T>GCA2615589705MRE11c.545-7A>C (n.545-7A>C)
c.554-7A>C (n.554-7A>C)
c.77-7A>C (n.77-7A>C)
n.841-7A>C
 gnomAD v4
11g.94476411G>ACA2574952839MRE11c.545-8C>T (n.545-8C>T)
c.554-8C>T (n.554-8C>T)
c.77-8C>T (n.77-8C>T)
n.841-8C>T
11g.94476411G>TCA2615589706MRE11c.545-8C>A (n.545-8C>A)
c.554-8C>A (n.554-8C>A)
c.77-8C>A (n.77-8C>A)
n.841-8C>A
 gnomAD v4
11g.94476412G>CCA1992433431MRE11c.545-9C>G (n.545-9C>G)
c.554-9C>G (n.554-9C>G)
c.77-9C>G (n.77-9C>G)
n.841-9C>G
 dbSNP
11g.94476412G=CA1992433433MRE11c.545-9C= (n.545-9C=)
c.554-9C= (n.554-9C=)
c.77-9C= (n.77-9C=)
n.841-9C=
11g.94476412G>TCA288180MRE11c.545-9C>A (n.545-9C>A)
c.554-9C>A (n.554-9C>A)
c.77-9C>A (n.77-9C>A)
n.841-9C>A
 ClinVar dbSNP gnomAD v4
11g.94476412_94476417delinsGACATTCA1992433428MRE11c.545-14_545-9delinsAATGTC (n.545-14_545-9delinsAATGTC)
c.554-14_554-9delinsAATGTC (n.554-14_554-9delinsAATGTC)
c.77-14_77-9delinsAATGTC (n.77-14_77-9delinsAATGTC)
n.841-14_841-9delinsAATGTC
11g.94476413A=CA1992433436MRE11c.545-10T= (n.545-10T=)
c.554-10T= (n.554-10T=)
c.77-10T= (n.77-10T=)
n.841-10T=
11g.94476413A>GCA600841623MRE11c.545-10T>C (n.545-10T>C)
c.554-10T>C (n.554-10T>C)
c.77-10T>C (n.77-10T>C)
n.841-10T>C
 dbSNP gnomAD v2
11g.94476419_94476423delCA600841622MRE11c.545-14_545-10del (n.545-14_545-10del)
c.554-14_554-10del (n.554-14_554-10del)
c.77-14_77-10del (n.77-14_77-10del)
n.841-14_841-10del
 dbSNP gnomAD v2 gnomAD v4
11g.94476414C=CA1992433437MRE11c.545-11G= (n.545-11G=)
c.554-11G= (n.554-11G=)
c.77-11G= (n.77-11G=)
n.841-11G=
11g.94476414C>TCA6235359MRE11c.545-11G>A (n.545-11G>A)
c.554-11G>A (n.554-11G>A)
c.77-11G>A (n.77-11G>A)
n.841-11G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476415A>TCA2574952841MRE11c.545-12T>A (n.545-12T>A)
c.554-12T>A (n.554-12T>A)
c.77-12T>A (n.77-12T>A)
n.841-12T>A
11g.94476416T>CCA6235360MRE11c.545-13A>G (n.545-13A>G)
c.554-13A>G (n.554-13A>G)
c.77-13A>G (n.77-13A>G)
n.841-13A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.94476416T=CA1992433439MRE11c.545-13A= (n.545-13A=)
c.554-13A= (n.554-13A=)
c.77-13A= (n.77-13A=)
n.841-13A=
11g.94476417delCA2615589716MRE11c.545-13del (n.545-13del)
c.554-13del (n.554-13del)
c.77-13del (n.77-13del)
n.841-13del
 gnomAD v4
11g.94476417T>ACA2615589718MRE11c.545-14A>T (n.545-14A>T)
c.554-14A>T (n.554-14A>T)
c.77-14A>T (n.77-14A>T)
n.841-14A>T
 gnomAD v4
11g.94476417T>CCA2615589719MRE11c.545-14A>G (n.545-14A>G)
c.554-14A>G (n.554-14A>G)
c.77-14A>G (n.77-14A>G)
n.841-14A>G
 gnomAD v4
11g.94476420A=CA1992433448MRE11c.545-17T= (n.545-17T=)
c.554-17T= (n.554-17T=)
c.77-17T= (n.77-17T=)
n.841-17T=
11g.94476420A>GCA6235361MRE11c.545-17T>C (n.545-17T>C)
c.554-17T>C (n.554-17T>C)
c.77-17T>C (n.77-17T>C)
n.841-17T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476421T>GCA654062456MRE11c.545-18A>C (n.545-18A>C)
c.554-18A>C (n.554-18A>C)
c.77-18A>C (n.77-18A>C)
n.841-18A>C
 COSMIC
11g.94476422dupCA941024555MRE11c.545-18dup (n.545-18dup)
c.554-18dup (n.554-18dup)
c.77-18dup (n.77-18dup)
n.841-18dup
 dbSNP gnomAD v3 gnomAD v4
11g.94476424T>ACA1992433453MRE11c.545-21A>T (n.545-21A>T)
c.554-21A>T (n.554-21A>T)
c.77-21A>T (n.77-21A>T)
n.841-21A>T
 dbSNP
11g.94476424T=CA1992433454MRE11c.545-21A= (n.545-21A=)
c.554-21A= (n.554-21A=)
c.77-21A= (n.77-21A=)
n.841-21A=
11g.94476426T>CCA6235362MRE11c.545-23A>G (n.545-23A>G)
c.554-23A>G (n.554-23A>G)
c.77-23A>G (n.77-23A>G)
n.841-23A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476426T=CA1992433455MRE11c.545-23A= (n.545-23A=)
c.554-23A= (n.554-23A=)
c.77-23A= (n.77-23A=)
n.841-23A=
11g.94476428T>CCA600841624MRE11c.545-25A>G (n.545-25A>G)
c.554-25A>G (n.554-25A>G)
c.77-25A>G (n.77-25A>G)
n.841-25A>G
 dbSNP gnomAD v2 gnomAD v4
11g.94476428T=CA1992433457MRE11c.545-25A= (n.545-25A=)
c.554-25A= (n.554-25A=)
c.77-25A= (n.77-25A=)
n.841-25A=
11g.94476430A=CA1992433458MRE11c.545-27T= (n.545-27T=)
c.554-27T= (n.554-27T=)
c.77-27T= (n.77-27T=)
n.841-27T=
11g.94476430A>CCA1992433459MRE11c.545-27T>G (n.545-27T>G)
c.554-27T>G (n.554-27T>G)
c.77-27T>G (n.77-27T>G)
n.841-27T>G
 dbSNP gnomAD v4
11g.94476432T>ACA1992433462MRE11c.545-29A>T (n.545-29A>T)
c.554-29A>T (n.554-29A>T)
c.77-29A>T (n.77-29A>T)
n.841-29A>T
 dbSNP gnomAD v4
11g.94476432T>CCA6235363MRE11c.545-29A>G (n.545-29A>G)
c.554-29A>G (n.554-29A>G)
c.77-29A>G (n.77-29A>G)
n.841-29A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.94476432T=CA1992433461MRE11c.545-29A= (n.545-29A=)
c.554-29A= (n.554-29A=)
c.77-29A= (n.77-29A=)
n.841-29A=
11g.94476434G=CA1992433465MRE11c.545-31C= (n.545-31C=)
c.554-31C= (n.554-31C=)
c.77-31C= (n.77-31C=)
n.841-31C=
11g.94476434G>TCA600841625MRE11c.545-31C>A (n.545-31C>A)
c.554-31C>A (n.554-31C>A)
c.77-31C>A (n.77-31C>A)
n.841-31C>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.94476436_94476439delinsTTTCCA1992433466MRE11c.545-36_545-33delinsGAAA (n.545-36_545-33delinsGAAA)
c.554-36_554-33delinsGAAA (n.554-36_554-33delinsGAAA)
c.77-36_77-33delinsGAAA (n.77-36_77-33delinsGAAA)
n.841-36_841-33delinsGAAA
11g.94476439_94476441delCA1992433469MRE11c.545-36_545-34del (n.545-36_545-34del)
c.554-36_554-34del (n.554-36_554-34del)
c.77-36_77-34del (n.77-36_77-34del)
n.841-36_841-34del
 dbSNP
11g.94476438T>CCA2615589725MRE11c.545-35A>G (n.545-35A>G)
c.554-35A>G (n.554-35A>G)
c.77-35A>G (n.77-35A>G)
n.841-35A>G
 gnomAD v4
11g.94476438_94476439insTAGTATATATTAATACCA2793218206MRE11c.545-36_545-35insGTATTAATATATACTA (n.545-36_545-35insGTATTAATATATACTA)
c.554-36_554-35insGTATTAATATATACTA (n.554-36_554-35insGTATTAATATATACTA)
c.77-36_77-35insGTATTAATATATACTA (n.77-36_77-35insGTATTAATATATACTA)
n.841-36_841-35insGTATTAATATATACTA
11g.94476439C>ACA6235364MRE11c.545-36G>T (n.545-36G>T)
c.554-36G>T (n.554-36G>T)
c.77-36G>T (n.77-36G>T)
n.841-36G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476439C=CA1992433471MRE11c.545-36G= (n.545-36G=)
c.554-36G= (n.554-36G=)
c.77-36G= (n.77-36G=)
n.841-36G=
11g.94476440T>CCA226532705MRE11c.545-37A>G (n.545-37A>G)
c.554-37A>G (n.554-37A>G)
c.77-37A>G (n.77-37A>G)
n.841-37A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.94476440T=CA1992433475MRE11c.545-37A= (n.545-37A=)
c.554-37A= (n.554-37A=)
c.77-37A= (n.77-37A=)
n.841-37A=
11g.94476440_94476441insACAAGAATATTTGTAACATAAGGATAAGGCACA2793218207MRE11c.545-38_545-37insTGCCTTATCCTTATGTTACAAATATTCTTGT (n.545-38_545-37insTGCCTTATCCTTATGTTACAAATATTCTTGT)
c.554-38_554-37insTGCCTTATCCTTATGTTACAAATATTCTTGT (n.554-38_554-37insTGCCTTATCCTTATGTTACAAATATTCTTGT)
c.77-38_77-37insTGCCTTATCCTTATGTTACAAATATTCTTGT (n.77-38_77-37insTGCCTTATCCTTATGTTACAAATATTCTTGT)
n.841-38_841-37insTGCCTTATCCTTATGTTACAAATATTCTTGT
11g.94476441T>CCA6235365MRE11c.545-38A>G (n.545-38A>G)
c.554-38A>G (n.554-38A>G)
c.77-38A>G (n.77-38A>G)
n.841-38A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.94476441T=CA1992433478MRE11c.545-38A= (n.545-38A=)
c.554-38A= (n.554-38A=)
c.77-38A= (n.77-38A=)
n.841-38A=
11g.94476442A>TCA2615589728MRE11c.545-39T>A (n.545-39T>A)
c.554-39T>A (n.554-39T>A)
c.77-39T>A (n.77-39T>A)
n.841-39T>A
 gnomAD v4
11g.94476443C>TCA2615589730MRE11c.545-40G>A (n.545-40G>A)
c.554-40G>A (n.554-40G>A)
c.77-40G>A (n.77-40G>A)
n.841-40G>A
 gnomAD v4
11g.94476444T>CCA2615589731MRE11c.545-41A>G (n.545-41A>G)
c.554-41A>G (n.554-41A>G)
c.77-41A>G (n.77-41A>G)
n.841-41A>G
 gnomAD v4

Number of alleles fetched