Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.108251897_108260359delCA916080444ATMc.1668_2466+1284del
c.1503_2301+1284del
c.624_1422+1284del
c.360_1158+1284del
n.2401_3199+1284del
ClinVar
11g.108258911A>GCA228399655ATMc.2377-75A>G (p.=)
c.2212-75A>G (p.=)
c.1333-75A>G (p.=)
c.1069-75A>G (p.=)
n.3110-75A>G
dbSNP
11g.108258912G>CCA942016471ATMc.2377-74G>C (p.=)
c.2212-74G>C (p.=)
c.1333-74G>C (p.=)
c.1069-74G>C (p.=)
n.3110-74G>C
11g.108258913A>GCA476672796ATMc.2377-73A>G (p.=)
c.2212-73A>G (p.=)
c.1333-73A>G (p.=)
c.1069-73A>G (p.=)
n.3110-73A>G
11g.108258918A>CCA671400907ATMc.2377-68A>C (p.=)
c.2212-68A>C (p.=)
c.1333-68A>C (p.=)
c.1069-68A>C (p.=)
n.3110-68A>C
11g.108258919C>TCA228399670ATMc.2377-67C>T (p.=)
c.2212-67C>T (p.=)
c.1333-67C>T (p.=)
c.1069-67C>T (p.=)
n.3110-67C>T
dbSNP
11g.108258920A>GCA601696597ATMc.2377-66A>G (p.=)
c.2212-66A>G (p.=)
c.1333-66A>G (p.=)
c.1069-66A>G (p.=)
n.3110-66A>G
gnomAD
11g.108258923G>CCA671400919ATMc.2377-63G>C (p.=)
c.2212-63G>C (p.=)
c.1333-63G>C (p.=)
c.1069-63G>C (p.=)
n.3110-63G>C
11g.108258926T>ACA228399675ATMc.2377-60T>A (p.=)
c.2212-60T>A (p.=)
c.1333-60T>A (p.=)
c.1069-60T>A (p.=)
n.3110-60T>A
dbSNP
11g.108258928C>ACA671400924ATMc.2377-58C>A (p.=)
c.2212-58C>A (p.=)
c.1333-58C>A (p.=)
c.1069-58C>A (p.=)
n.3110-58C>A
11g.108258929C>TCA671400927ATMc.2377-57C>T (p.=)
c.2212-57C>T (p.=)
c.1333-57C>T (p.=)
c.1069-57C>T (p.=)
n.3110-57C>T
11g.108258930A>GCA15683344ATMc.2377-56A>G (p.=)
c.2212-56A>G (p.=)
c.1333-56A>G (p.=)
c.1069-56A>G (p.=)
n.3110-56A>G
dbSNP gnomAD
11g.108258930A>TCA671400930ATMc.2377-56A>T (p.=)
c.2212-56A>T (p.=)
c.1333-56A>T (p.=)
c.1069-56A>T (p.=)
n.3110-56A>T
11g.108258934A>GCA228399687ATMc.2377-52A>G (p.=)
c.2212-52A>G (p.=)
c.1333-52A>G (p.=)
c.1069-52A>G (p.=)
n.3110-52A>G
dbSNP
11g.108258936A>CCA601696600ATMc.2377-50A>C (p.=)
c.2212-50A>C (p.=)
c.1333-50A>C (p.=)
c.1069-50A>C (p.=)
n.3110-50A>C
gnomAD
11g.108258937A>TCA6265011ATMc.2377-49A>T (p.=)
c.2212-49A>T (p.=)
c.1333-49A>T (p.=)
c.1069-49A>T (p.=)
n.3110-49A>T
dbSNP ExAC gnomAD
11g.108258941T>ACA6265012ATMc.2377-45T>A (p.=)
c.2212-45T>A (p.=)
c.1333-45T>A (p.=)
c.1069-45T>A (p.=)
n.3110-45T>A
dbSNP ExAC
11g.108258949dupCA671400934ATMc.2377-37dup (p.=)
c.2212-37dup (p.=)
c.1333-37dup (p.=)
c.1069-37dup (p.=)
n.3110-37dup
dbSNP
11g.108258948T>GCA228399703ATMc.2377-38T>G (p.=)
c.2212-38T>G (p.=)
c.1333-38T>G (p.=)
c.1069-38T>G (p.=)
n.3110-38T>G
dbSNP gnomAD
11g.108258957_108258971delCA601696602ATMc.2377-29_2377-15del (p.=)
c.2212-29_2212-15del (p.=)
c.1333-29_1333-15del (p.=)
c.1069-29_1069-15del (p.=)
n.3110-29_3110-15del
dbSNP gnomAD
11g.108258950C>GCA671400943ATMc.2377-36C>G (p.=)
c.2212-36C>G (p.=)
c.1333-36C>G (p.=)
c.1069-36C>G (p.=)
n.3110-36C>G
11g.108258950C>TCA601696605ATMc.2377-36C>T (p.=)
c.2212-36C>T (p.=)
c.1333-36C>T (p.=)
c.1069-36C>T (p.=)
n.3110-36C>T
gnomAD
11g.108258952T>CCA6265013ATMc.2377-34T>C (p.=)
c.2212-34T>C (p.=)
c.1333-34T>C (p.=)
c.1069-34T>C (p.=)
n.3110-34T>C
dbSNP ExAC gnomAD
11g.108258957G>CCA6265014ATMc.2377-29G>C (p.=)
c.2212-29G>C (p.=)
c.1333-29G>C (p.=)
c.1069-29G>C (p.=)
n.3110-29G>C
dbSNP ExAC gnomAD
11g.108258967_108258968delCA918963772ATMc.2377-19_2377-18del (p.=)
c.2212-19_2212-18del (p.=)
c.1333-19_1333-18del (p.=)
c.1069-19_1069-18del (p.=)
n.3110-19_3110-18del
dbSNP
11g.108258971_108258974delCA298012ATMc.2377-15_2377-12del (p.=)
c.2212-15_2212-12del (p.=)
c.1333-15_1333-12del (p.=)
c.1069-15_1069-12del (p.=)
n.3110-15_3110-12del
ClinVar dbSNP ExAC gnomAD
11g.108258967T>GCA6265015ATMc.2377-19T>G (p.=)
c.2212-19T>G (p.=)
c.1333-19T>G (p.=)
c.1069-19T>G (p.=)
n.3110-19T>G
ClinVar dbSNP ExAC gnomAD
11g.108258968T>CCA6265016ATMc.2377-18T>C (p.=)
c.2212-18T>C (p.=)
c.1333-18T>C (p.=)
c.1069-18T>C (p.=)
n.3110-18T>C
ClinVar dbSNP ExAC gnomAD
11g.108258969G>CCA1139662169ATMc.2377-17G>C (p.=)
c.2212-17G>C (p.=)
c.1333-17G>C (p.=)
c.1069-17G>C (p.=)
n.3110-17G>C
ClinVar
11g.108258969G>TCA6265017ATMc.2377-17G>T (p.=)
c.2212-17G>T (p.=)
c.1333-17G>T (p.=)
c.1069-17G>T (p.=)
n.3110-17G>T
dbSNP ExAC
11g.108258970T>ACA228399748ATMc.2377-16T>A (p.=)
c.2212-16T>A (p.=)
c.1333-16T>A (p.=)
c.1069-16T>A (p.=)
n.3110-16T>A
dbSNP gnomAD
11g.108258971T>CCA913188491ATMc.2377-15T>C (p.=)
c.2212-15T>C (p.=)
c.1333-15T>C (p.=)
c.1069-15T>C (p.=)
n.3110-15T>C
ClinVar
11g.108258973G>CCA601696610ATMc.2377-13G>C (p.=)
c.2212-13G>C (p.=)
c.1333-13G>C (p.=)
c.1069-13G>C (p.=)
n.3110-13G>C
gnomAD
11g.108258975C>GCA913188492ATMc.2377-11C>G (p.=)
c.2212-11C>G (p.=)
c.1333-11C>G (p.=)
c.1069-11C>G (p.=)
n.3110-11C>G
ClinVar
11g.108258977T>ACA1139662170ATMc.2377-9T>A (p.=)
c.2212-9T>A (p.=)
c.1333-9T>A (p.=)
c.1069-9T>A (p.=)
n.3110-9T>A
ClinVar
11g.108258979A>GCA913188493ATMc.2377-7A>G (p.=)
c.2212-7A>G (p.=)
c.1333-7A>G (p.=)
c.1069-7A>G (p.=)
n.3110-7A>G
ClinVar
11g.108258980T>ACA10577426ATMc.2377-6T>A (p.=)
c.2212-6T>A (p.=)
c.1333-6T>A (p.=)
c.1069-6T>A (p.=)
n.3110-6T>A
ClinVar dbSNP gnomAD
11g.108258981T>CCA6265018ATMc.2377-5T>C (p.=)
c.2212-5T>C (p.=)
c.1333-5T>C (p.=)
c.1069-5T>C (p.=)
n.3110-5T>C
ClinVar dbSNP ExAC gnomAD
11g.108258984A>CCA382540983ATMc.2377-2A>C (p.=)
c.2212-2A>C (p.=)
c.1333-2A>C (p.=)
c.1069-2A>C (p.=)
n.3110-2A>C
11g.108258984A>GCA16041391ATMc.2377-2A>G (p.=)
c.2212-2A>G (p.=)
c.1333-2A>G (p.=)
c.1069-2A>G (p.=)
n.3110-2A>G
ClinVar dbSNP
11g.108258984A>TCA382540985ATMc.2377-2A>T (p.=)
c.2212-2A>T (p.=)
c.1333-2A>T (p.=)
c.1069-2A>T (p.=)
n.3110-2A>T
11g.108258985G>ACA382540989ATMc.2377-1G>A (p.=)
c.2212-1G>A (p.=)
c.1333-1G>A (p.=)
c.1069-1G>A (p.=)
n.3110-1G>A
COSMIC COSMIC
11g.108258985G>CCA382540992ATMc.2377-1G>C (p.=)
c.2212-1G>C (p.=)
c.1333-1G>C (p.=)
c.1069-1G>C (p.=)
n.3110-1G>C
11g.108258985G>TCA382540993ATMc.2377-1G>T (p.=)
c.2212-1G>T (p.=)
c.1333-1G>T (p.=)
c.1069-1G>T (p.=)
n.3110-1G>T
11g.108258986A>CCA382540996ATMc.2377A>C (p.Lys793Gln)
c.2212A>C (p.Lys738Gln)
c.1333A>C (p.Lys445Gln)
c.1069A>C (p.Lys357Gln)
n.3110A>C
ClinVar
11g.108258986A>GCA164793ATMc.2377A>G (p.Lys793Glu)
c.2212A>G (p.Lys738Glu)
c.1333A>G (p.Lys445Glu)
c.1069A>G (p.Lys357Glu)
n.3110A>G
ClinVar dbSNP gnomAD
11g.108258986A>TCA382540998ATMc.2377A>T (p.Lys793Ter)
c.2212A>T (p.Lys738Ter)
c.1333A>T (p.Lys445Ter)
c.1069A>T (p.Lys357Ter)
n.3110A>T
11g.108258986_108258987dupCA16041392ATMc.2377_2378dup (p.Ser794ArgfsTer15)
c.2212_2213dup (p.Ser739ArgfsTer15)
c.1333_1334dup (p.Ser446ArgfsTer15)
c.1069_1070dup (p.Ser358ArgfsTer15)
n.3110_3111dup
ClinVar dbSNP
11g.108258987A>CCA382541004ATMc.2378A>C (p.Lys793Thr)
c.2213A>C (p.Lys738Thr)
c.1334A>C (p.Lys445Thr)
c.1070A>C (p.Lys357Thr)
n.3111A>C
11g.108258987A>GCA382541002ATMc.2378A>G (p.Lys793Arg)
c.2213A>G (p.Lys738Arg)
c.1334A>G (p.Lys445Arg)
c.1070A>G (p.Lys357Arg)
n.3111A>G
COSMIC COSMIC

Number of alleles fetched