Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.108251797A>GCA601695561ATMc.1608-40A>G (p.=)
c.1443-40A>G (p.=)
c.564-40A>G (p.=)
c.300-40A>G (p.=)
n.2341-40A>G
gnomAD
11g.108251798A>GCA6264844ATMc.1608-39A>G (p.=)
c.1443-39A>G (p.=)
c.564-39A>G (p.=)
c.300-39A>G (p.=)
n.2341-39A>G
dbSNP ExAC gnomAD
11g.108251799T>CCA601695562ATMc.1608-38T>C (p.=)
c.1443-38T>C (p.=)
c.564-38T>C (p.=)
c.300-38T>C (p.=)
n.2341-38T>C
gnomAD
11g.108251800A>GCA671376003ATMc.1608-37A>G (p.=)
c.1443-37A>G (p.=)
c.564-37A>G (p.=)
c.300-37A>G (p.=)
n.2341-37A>G
11g.108251811C>TCA601695563ATMc.1608-26C>T (p.=)
c.1443-26C>T (p.=)
c.564-26C>T (p.=)
c.300-26C>T (p.=)
n.2341-26C>T
gnomAD
11g.108251813C>ACA6264845ATMc.1608-24C>A (p.=)
c.1443-24C>A (p.=)
c.564-24C>A (p.=)
c.300-24C>A (p.=)
n.2341-24C>A
dbSNP ExAC gnomAD
11g.108251814A>GCA6264846ATMc.1608-23A>G (p.=)
c.1443-23A>G (p.=)
c.564-23A>G (p.=)
c.300-23A>G (p.=)
n.2341-23A>G
dbSNP ExAC gnomAD
11g.108251815A>GCA6264847ATMc.1608-22A>G (p.=)
c.1443-22A>G (p.=)
c.564-22A>G (p.=)
c.300-22A>G (p.=)
n.2341-22A>G
dbSNP ExAC gnomAD
11g.108251815A>TCA6264848ATMc.1608-22A>T (p.=)
c.1443-22A>T (p.=)
c.564-22A>T (p.=)
c.300-22A>T (p.=)
n.2341-22A>T
dbSNP ExAC gnomAD
11g.108251817T>CCA601695564ATMc.1608-20T>C (p.=)
c.1443-20T>C (p.=)
c.564-20T>C (p.=)
c.300-20T>C (p.=)
n.2341-20T>C
gnomAD
11g.108251818G>TCA6264849ATMc.1608-19G>T (p.=)
c.1443-19G>T (p.=)
c.564-19G>T (p.=)
c.300-19G>T (p.=)
n.2341-19G>T
ClinVar dbSNP ExAC gnomAD
11g.108251821C>TCA1139662157ATMc.1608-16C>T (p.=)
c.1443-16C>T (p.=)
c.564-16C>T (p.=)
c.300-16C>T (p.=)
n.2341-16C>T
ClinVar
11g.108251825G>ACA6264850ATMc.1608-12G>A (p.=)
c.1443-12G>A (p.=)
c.564-12G>A (p.=)
c.300-12G>A (p.=)
n.2341-12G>A
dbSNP ExAC gnomAD
11g.108251825G>CCA601695565ATMc.1608-12G>C (p.=)
c.1443-12G>C (p.=)
c.564-12G>C (p.=)
c.300-12G>C (p.=)
n.2341-12G>C
ClinVar gnomAD
11g.108251829delCA16619120ATMc.1608-8del (p.=)
c.1443-8del (p.=)
c.564-8del (p.=)
c.300-8del (p.=)
n.2341-8del
ClinVar dbSNP
11g.108251829T>CCA6264851ATMc.1608-8T>C (p.=)
c.1443-8T>C (p.=)
c.564-8T>C (p.=)
c.300-8T>C (p.=)
n.2341-8T>C
ClinVar dbSNP ExAC gnomAD
11g.108251830G>ACA658683712ATMc.1608-7G>A (p.=)
c.1443-7G>A (p.=)
c.564-7G>A (p.=)
c.300-7G>A (p.=)
n.2341-7G>A
ClinVar
11g.108251831T>GCA1139662158ATMc.1608-6T>G (p.=)
c.1443-6T>G (p.=)
c.564-6T>G (p.=)
c.300-6T>G (p.=)
n.2341-6T>G
ClinVar
11g.108251833A>GCA913188409ATMc.1608-4A>G (p.=)
c.1443-4A>G (p.=)
c.564-4A>G (p.=)
c.300-4A>G (p.=)
n.2341-4A>G
ClinVar
11g.108251834T>CCA6264852ATMc.1608-3T>C (p.=)
c.1443-3T>C (p.=)
c.564-3T>C (p.=)
c.300-3T>C (p.=)
n.2341-3T>C
ClinVar dbSNP ExAC gnomAD
11g.108251835A>CCA382534464ATMc.1608-2A>C (p.=)
c.1443-2A>C (p.=)
c.564-2A>C (p.=)
c.300-2A>C (p.=)
n.2341-2A>C
11g.108251835A>GCA382534462ATMc.1608-2A>G (p.=)
c.1443-2A>G (p.=)
c.564-2A>G (p.=)
c.300-2A>G (p.=)
n.2341-2A>G
11g.108251835A>TCA382534463ATMc.1608-2A>T (p.=)
c.1443-2A>T (p.=)
c.564-2A>T (p.=)
c.300-2A>T (p.=)
n.2341-2A>T
11g.108251836G>ACA382534465ATMc.1608-1G>A (p.=)
c.1443-1G>A (p.=)
c.564-1G>A (p.=)
c.300-1G>A (p.=)
n.2341-1G>A
ClinVar COSMIC COSMIC
11g.108251836G>CCA382534466ATMc.1608-1G>C (p.=)
c.1443-1G>C (p.=)
c.564-1G>C (p.=)
c.300-1G>C (p.=)
n.2341-1G>C
ClinVar
11g.108251836G>TCA382534467ATMc.1608-1G>T (p.=)
c.1443-1G>T (p.=)
c.564-1G>T (p.=)
c.300-1G>T (p.=)
n.2341-1G>T
11g.108251837T>ACA382534468ATMc.1608T>A (p.Cys536Ter)
c.1443T>A (p.Cys481Ter)
c.564T>A (p.Cys188Ter)
c.300T>A (p.Cys100Ter)
n.2341T>A
11g.108251837T>CCA476672022ATMc.1608T>C (p.Cys536=)
c.1443T>C (p.Cys481=)
c.564T>C (p.Cys188=)
c.300T>C (p.Cys100=)
n.2341T>C
11g.108251837T>GCA382534469ATMc.1608T>G (p.Cys536Trp)
c.1443T>G (p.Cys481Trp)
c.564T>G (p.Cys188Trp)
c.300T>G (p.Cys100Trp)
n.2341T>G
11g.108251838C>ACA382534470ATMc.1609C>A (p.Pro537Thr)
c.1444C>A (p.Pro482Thr)
c.565C>A (p.Pro189Thr)
c.301C>A (p.Pro101Thr)
n.2342C>A
11g.108251838C>GCA382534471ATMc.1609C>G (p.Pro537Ala)
c.1444C>G (p.Pro482Ala)
c.565C>G (p.Pro189Ala)
c.301C>G (p.Pro101Ala)
n.2342C>G
11g.108251838C>TCA382534472ATMc.1609C>T (p.Pro537Ser)
c.1444C>T (p.Pro482Ser)
c.565C>T (p.Pro189Ser)
c.301C>T (p.Pro101Ser)
n.2342C>T
ClinVar gnomAD
11g.108251838_108251890delCA658655584ATMc.1609_1661del (p.Pro537GlyfsTer11)
c.1444_1496del (p.Pro482GlyfsTer11)
c.565_617del (p.Pro189GlyfsTer11)
c.301_353del (p.Pro101GlyfsTer11)
n.2342_2394del
11g.108251839C>ACA168348ATMc.1610C>A (p.Pro537His)
c.1445C>A (p.Pro482His)
c.566C>A (p.Pro189His)
c.302C>A (p.Pro101His)
n.2343C>A
ClinVar dbSNP
11g.108251839C>GCA382534473ATMc.1610C>G (p.Pro537Arg)
c.1445C>G (p.Pro482Arg)
c.566C>G (p.Pro189Arg)
c.302C>G (p.Pro101Arg)
n.2343C>G
11g.108251839C>TCA382534474ATMc.1610C>T (p.Pro537Leu)
c.1445C>T (p.Pro482Leu)
c.566C>T (p.Pro189Leu)
c.302C>T (p.Pro101Leu)
n.2343C>T
ClinVar
11g.108251840T>ACA476672023ATMc.1611T>A (p.Pro537=)
c.1446T>A (p.Pro482=)
c.567T>A (p.Pro189=)
c.303T>A (p.Pro101=)
n.2344T>A
11g.108251840T>CCA476672024ATMc.1611T>C (p.Pro537=)
c.1446T>C (p.Pro482=)
c.567T>C (p.Pro189=)
c.303T>C (p.Pro101=)
n.2344T>C
11g.108251840T>GCA476672025ATMc.1611T>G (p.Pro537=)
c.1446T>G (p.Pro482=)
c.567T>G (p.Pro189=)
c.303T>G (p.Pro101=)
n.2344T>G
11g.108251841G>ACA382534477ATMc.1612G>A (p.Ala538Thr)
c.1447G>A (p.Ala483Thr)
c.568G>A (p.Ala190Thr)
c.304G>A (p.Ala102Thr)
n.2345G>A
11g.108251841G>CCA382534476ATMc.1612G>C (p.Ala538Pro)
c.1447G>C (p.Ala483Pro)
c.568G>C (p.Ala190Pro)
c.304G>C (p.Ala102Pro)
n.2345G>C
ClinVar
11g.108251841G>TCA382534475ATMc.1612G>T (p.Ala538Ser)
c.1447G>T (p.Ala483Ser)
c.568G>T (p.Ala190Ser)
c.304G>T (p.Ala102Ser)
n.2345G>T
11g.108251841_108251842delinsTTCA913188410ATMc.1612_1613delinsTT (p.Ala538Leu)
c.1447_1448delinsTT (p.Ala483Leu)
c.568_569delinsTT (p.Ala190Leu)
c.304_305delinsTT (p.Ala102Leu)
n.2345_2346delinsTT
ClinVar
11g.108251842C>ACA382534478ATMc.1613C>A (p.Ala538Glu)
c.1448C>A (p.Ala483Glu)
c.569C>A (p.Ala190Glu)
c.305C>A (p.Ala102Glu)
n.2346C>A
11g.108251842C>GCA382534479ATMc.1613C>G (p.Ala538Gly)
c.1448C>G (p.Ala483Gly)
c.569C>G (p.Ala190Gly)
c.305C>G (p.Ala102Gly)
n.2346C>G
11g.108251842C>TCA382534480ATMc.1613C>T (p.Ala538Val)
c.1448C>T (p.Ala483Val)
c.569C>T (p.Ala190Val)
c.305C>T (p.Ala102Val)
n.2346C>T
ClinVar
11g.108251843A>CCA476672026ATMc.1614A>C (p.Ala538=)
c.1449A>C (p.Ala483=)
c.570A>C (p.Ala190=)
c.306A>C (p.Ala102=)
n.2347A>C
11g.108251843A>GCA10579017ATMc.1614A>G (p.Ala538=)
c.1449A>G (p.Ala483=)
c.570A>G (p.Ala190=)
c.306A>G (p.Ala102=)
n.2347A>G
ClinVar dbSNP
11g.108251843A>TCA476672027ATMc.1614A>T (p.Ala538=)
c.1449A>T (p.Ala483=)
c.570A>T (p.Ala190=)
c.306A>T (p.Ala102=)
n.2347A>T
11g.108251844G>ACA382534481ATMc.1615G>A (p.Val539Ile)
c.1450G>A (p.Val484Ile)
c.571G>A (p.Val191Ile)
c.307G>A (p.Val103Ile)
n.2348G>A

Number of alleles fetched