Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.108251895A>CCA382535095ATMc.1666A>C (p.Lys556Gln)
c.1501A>C (p.Lys501Gln)
c.622A>C (p.Lys208Gln)
c.358A>C (p.Lys120Gln)
n.2399A>C
11g.108251895A>GCA382535096ATMc.1666A>G (p.Lys556Glu)
c.1501A>G (p.Lys501Glu)
c.622A>G (p.Lys208Glu)
c.358A>G (p.Lys120Glu)
n.2399A>G
11g.108251895A>TCA382535098ATMc.1666A>T (p.Lys556Ter)
c.1501A>T (p.Lys501Ter)
c.622A>T (p.Lys208Ter)
c.358A>T (p.Lys120Ter)
n.2399A>T
11g.108251897_108260359delCA916080444ATMc.1668_2466+1284del
c.1503_2301+1284del
c.624_1422+1284del
c.360_1158+1284del
n.2401_3199+1284del
ClinVar
11g.108251896A>CCA382535100ATMc.1667A>C (p.Lys556Thr)
c.1502A>C (p.Lys501Thr)
c.623A>C (p.Lys208Thr)
c.359A>C (p.Lys120Thr)
n.2400A>C
11g.108251896A>GCA382535102ATMc.1667A>G (p.Lys556Arg)
c.1502A>G (p.Lys501Arg)
c.623A>G (p.Lys208Arg)
c.359A>G (p.Lys120Arg)
n.2400A>G
11g.108251896A>TCA382535104ATMc.1667A>T (p.Lys556Ile)
c.1502A>T (p.Lys501Ile)
c.623A>T (p.Lys208Ile)
c.359A>T (p.Lys120Ile)
n.2400A>T
11g.108251897A>CCA228391789ATMc.1668A>C (p.Lys556Asn)
c.1503A>C (p.Lys501Asn)
c.624A>C (p.Lys208Asn)
c.360A>C (p.Lys120Asn)
n.2401A>C
dbSNP
11g.108251897A>GCA476672094ATMc.1668A>G (p.Lys556=)
c.1503A>G (p.Lys501=)
c.624A>G (p.Lys208=)
c.360A>G (p.Lys120=)
n.2401A>G
COSMIC COSMIC
11g.108251897A>TCA382535106ATMc.1668A>T (p.Lys556Asn)
c.1503A>T (p.Lys501Asn)
c.624A>T (p.Lys208Asn)
c.360A>T (p.Lys120Asn)
n.2401A>T
11g.108251898A>CCA382535110ATMc.1669A>C (p.Met557Leu)
c.1504A>C (p.Met502Leu)
c.625A>C (p.Met209Leu)
c.361A>C (p.Met121Leu)
n.2402A>C
11g.108251898A>GCA382535109ATMc.1669A>G (p.Met557Val)
c.1504A>G (p.Met502Val)
c.625A>G (p.Met209Val)
c.361A>G (p.Met121Val)
n.2402A>G
ClinVar gnomAD
11g.108251898A>TCA382535108ATMc.1669A>T (p.Met557Leu)
c.1504A>T (p.Met502Leu)
c.625A>T (p.Met209Leu)
c.361A>T (p.Met121Leu)
n.2402A>T
11g.108251899delCA645569721ATMc.1670del (p.Met557ArgfsTer3)
c.1505del (p.Met502ArgfsTer3)
c.626del (p.Met209ArgfsTer3)
c.362del (p.Met121ArgfsTer3)
n.2403del
COSMIC COSMIC
11g.108251899T>ACA382535113ATMc.1670T>A (p.Met557Lys)
c.1505T>A (p.Met502Lys)
c.626T>A (p.Met209Lys)
c.362T>A (p.Met121Lys)
n.2403T>A
11g.108251899T>CCA194138ATMc.1670T>C (p.Met557Thr)
c.1505T>C (p.Met502Thr)
c.626T>C (p.Met209Thr)
c.362T>C (p.Met121Thr)
n.2403T>C
ClinVar dbSNP
11g.108251899T>GCA382535111ATMc.1670T>G (p.Met557Arg)
c.1505T>G (p.Met502Arg)
c.626T>G (p.Met209Arg)
c.362T>G (p.Met121Arg)
n.2403T>G
ClinVar
11g.108251900G>ACA298141ATMc.1671G>A (p.Met557Ile)
c.1506G>A (p.Met502Ile)
c.627G>A (p.Met209Ile)
c.363G>A (p.Met121Ile)
n.2404G>A
ClinVar dbSNP gnomAD
11g.108251900G>CCA382535115ATMc.1671G>C (p.Met557Ile)
c.1506G>C (p.Met502Ile)
c.627G>C (p.Met209Ile)
c.363G>C (p.Met121Ile)
n.2404G>C
11g.108251900G>TCA382535116ATMc.1671G>T (p.Met557Ile)
c.1506G>T (p.Met502Ile)
c.627G>T (p.Met209Ile)
c.363G>T (p.Met121Ile)
n.2404G>T
11g.108251900_108251901delinsCCA645569722ATMc.1671_1672delinsC (p.Met557IlefsTer3)
c.1506_1507delinsC (p.Met502IlefsTer3)
c.627_628delinsC (p.Met209IlefsTer3)
c.363_364delinsC (p.Met121IlefsTer3)
n.2404_2405delinsC
COSMIC
11g.108251902dupCA671376343ATMc.1673dup (p.Ile559AsnfsTer7)
c.1508dup (p.Ile504AsnfsTer7)
c.629dup (p.Ile211AsnfsTer7)
c.365dup (p.Ile123AsnfsTer7)
n.2406dup
dbSNP
11g.108251901G>ACA382535127ATMc.1672G>A (p.Gly558Arg)
c.1507G>A (p.Gly503Arg)
c.628G>A (p.Gly210Arg)
c.364G>A (p.Gly122Arg)
n.2405G>A
11g.108251901G>CCA382535125ATMc.1672G>C (p.Gly558Arg)
c.1507G>C (p.Gly503Arg)
c.628G>C (p.Gly210Arg)
c.364G>C (p.Gly122Arg)
n.2405G>C
11g.108251901G>TCA382535124ATMc.1672G>T (p.Gly558Ter)
c.1507G>T (p.Gly503Ter)
c.628G>T (p.Gly210Ter)
c.364G>T (p.Gly122Ter)
n.2405G>T
COSMIC
11g.108251902G>ACA382535130ATMc.1673G>A (p.Gly558Glu)
c.1508G>A (p.Gly503Glu)
c.629G>A (p.Gly210Glu)
c.365G>A (p.Gly122Glu)
n.2406G>A
11g.108251902G>CCA382535131ATMc.1673G>C (p.Gly558Ala)
c.1508G>C (p.Gly503Ala)
c.629G>C (p.Gly210Ala)
c.365G>C (p.Gly122Ala)
n.2406G>C
ClinVar
11g.108251902G>TCA16619122ATMc.1673G>T (p.Gly558Val)
c.1508G>T (p.Gly503Val)
c.629G>T (p.Gly210Val)
c.365G>T (p.Gly122Val)
n.2406G>T
ClinVar COSMIC COSMIC
11g.108251903A>CCA476672098ATMc.1674A>C (p.Gly558=)
c.1509A>C (p.Gly503=)
c.630A>C (p.Gly210=)
c.366A>C (p.Gly122=)
n.2407A>C
11g.108251903A>GCA476672100ATMc.1674A>G (p.Gly558=)
c.1509A>G (p.Gly503=)
c.630A>G (p.Gly210=)
c.366A>G (p.Gly122=)
n.2407A>G
COSMIC COSMIC
11g.108251903A>TCA476672099ATMc.1674A>T (p.Gly558=)
c.1509A>T (p.Gly503=)
c.630A>T (p.Gly210=)
c.366A>T (p.Gly122=)
n.2407A>T
11g.108251904A>CCA382535133ATMc.1675A>C (p.Ile559Leu)
c.1510A>C (p.Ile504Leu)
c.631A>C (p.Ile211Leu)
c.367A>C (p.Ile123Leu)
n.2408A>C
11g.108251904A>GCA16613332ATMc.1675A>G (p.Ile559Val)
c.1510A>G (p.Ile504Val)
c.631A>G (p.Ile211Val)
c.367A>G (p.Ile123Val)
n.2408A>G
ClinVar gnomAD
11g.108251904A>TCA382535135ATMc.1675A>T (p.Ile559Leu)
c.1510A>T (p.Ile504Leu)
c.631A>T (p.Ile211Leu)
c.367A>T (p.Ile123Leu)
n.2408A>T
11g.108251905T>ACA382535136ATMc.1676T>A (p.Ile559Lys)
c.1511T>A (p.Ile504Lys)
c.632T>A (p.Ile211Lys)
c.368T>A (p.Ile123Lys)
n.2409T>A
11g.108251905T>CCA382535140ATMc.1676T>C (p.Ile559Thr)
c.1511T>C (p.Ile504Thr)
c.632T>C (p.Ile211Thr)
c.368T>C (p.Ile123Thr)
n.2409T>C
ClinVar
11g.108251905T>GCA382535138ATMc.1676T>G (p.Ile559Arg)
c.1511T>G (p.Ile504Arg)
c.632T>G (p.Ile211Arg)
c.368T>G (p.Ile123Arg)
n.2409T>G
11g.108251906A>CCA476672104ATMc.1677A>C (p.Ile559=)
c.1512A>C (p.Ile504=)
c.633A>C (p.Ile211=)
c.369A>C (p.Ile123=)
n.2410A>C
11g.108251906A>GCA382535142ATMc.1677A>G (p.Ile559Met)
c.1512A>G (p.Ile504Met)
c.633A>G (p.Ile211Met)
c.369A>G (p.Ile123Met)
n.2410A>G
ClinVar gnomAD
11g.108251906A>TCA476672106ATMc.1677A>T (p.Ile559=)
c.1512A>T (p.Ile504=)
c.633A>T (p.Ile211=)
c.369A>T (p.Ile123=)
n.2410A>T
11g.108251907G>ACA382535143ATMc.1678G>A (p.Glu560Lys)
c.1513G>A (p.Glu505Lys)
c.634G>A (p.Glu212Lys)
c.370G>A (p.Glu124Lys)
n.2411G>A
11g.108251907G>CCA382535144ATMc.1678G>C (p.Glu560Gln)
c.1513G>C (p.Glu505Gln)
c.634G>C (p.Glu212Gln)
c.370G>C (p.Glu124Gln)
n.2411G>C
11g.108251907G>TCA382535146ATMc.1678G>T (p.Glu560Ter)
c.1513G>T (p.Glu505Ter)
c.634G>T (p.Glu212Ter)
c.370G>T (p.Glu124Ter)
n.2411G>T
11g.108251908A>CCA382535148ATMc.1679A>C (p.Glu560Ala)
c.1514A>C (p.Glu505Ala)
c.635A>C (p.Glu212Ala)
c.371A>C (p.Glu124Ala)
n.2412A>C
11g.108251908A>GCA6264856ATMc.1679A>G (p.Glu560Gly)
c.1514A>G (p.Glu505Gly)
c.635A>G (p.Glu212Gly)
c.371A>G (p.Glu124Gly)
n.2412A>G
dbSNP ExAC gnomAD
11g.108251908A>TCA382535150ATMc.1679A>T (p.Glu560Val)
c.1514A>T (p.Glu505Val)
c.635A>T (p.Glu212Val)
c.371A>T (p.Glu124Val)
n.2412A>T
11g.108251909G>ACA476672111ATMc.1680G>A (p.Glu560=)
c.1515G>A (p.Glu505=)
c.636G>A (p.Glu212=)
c.372G>A (p.Glu124=)
n.2413G>A
ClinVar
11g.108251909G>CCA382535152ATMc.1680G>C (p.Glu560Asp)
c.1515G>C (p.Glu505Asp)
c.636G>C (p.Glu212Asp)
c.372G>C (p.Glu124Asp)
n.2413G>C
11g.108251909G>TCA382535153ATMc.1680G>T (p.Glu560Asp)
c.1515G>T (p.Glu505Asp)
c.636G>T (p.Glu212Asp)
c.372G>T (p.Glu124Asp)
n.2413G>T
11g.108251910C>ACA382535155ATMc.1681C>A (p.Gln561Lys)
c.1516C>A (p.Gln506Lys)
c.637C>A (p.Gln213Lys)
c.373C>A (p.Gln125Lys)
n.2414C>A

Number of alleles fetched