Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.55443828A>CCA439485251CLOCK,TMEM165c.1761T>G (p.Ser587=)
c.353-8411A>C
n.343T>G
c.409-8411A>C
c.899-8411A>C (n.899-8411A>C)
c.1584T>G (p.Ser528=)
4g.55443828A>GCA439485252CLOCK,TMEM165c.1761T>C (p.Ser587=)
c.353-8411A>G
n.343T>C
c.409-8411A>G
c.899-8411A>G (n.899-8411A>G)
c.1584T>C (p.Ser528=)
4g.55443828A>TCA439485253CLOCK,TMEM165c.1761T>A (p.Ser587=)
c.353-8411A>T
n.343T>A
c.409-8411A>T
c.899-8411A>T (n.899-8411A>T)
c.1584T>A (p.Ser528=)
4g.55443829G>ACA356916005CLOCK,TMEM165c.1760C>T (p.Ser587Phe)
c.353-8410G>A
n.342C>T
c.409-8410G>A
c.899-8410G>A (n.899-8410G>A)
c.1583C>T (p.Ser528Phe)
4g.55443829G>CCA356915997CLOCK,TMEM165c.1760C>G (p.Ser587Cys)
c.353-8410G>C
n.342C>G
c.409-8410G>C
c.899-8410G>C (n.899-8410G>C)
c.1583C>G (p.Ser528Cys)
4g.55443829G>TCA356916001CLOCK,TMEM165c.1760C>A (p.Ser587Tyr)
c.353-8410G>T
n.342C>A
c.409-8410G>T
c.899-8410G>T (n.899-8410G>T)
c.1583C>A (p.Ser528Tyr)
4g.55443831_55443833delCA2578091690CLOCK,TMEM165c.1758_1760del (p.Ser587del)
c.353-8408_353-8406del
n.340_342del
c.409-8408_409-8406del
c.899-8408_899-8406del (n.899-8408_899-8406del)
c.1581_1583del (p.Ser528del)
4g.55443830A>CCA356916006CLOCK,TMEM165c.1759T>G (p.Ser587Ala)
c.353-8409A>C
n.341T>G
c.409-8409A>C
c.899-8409A>C (n.899-8409A>C)
c.1582T>G (p.Ser528Ala)
4g.55443830A>GCA356916007CLOCK,TMEM165c.1759T>C (p.Ser587Pro)
c.353-8409A>G
n.341T>C
c.409-8409A>G
c.899-8409A>G (n.899-8409A>G)
c.1582T>C (p.Ser528Pro)
4g.55443830A>TCA356916008CLOCK,TMEM165c.1759T>A (p.Ser587Thr)
c.353-8409A>T
n.341T>A
c.409-8409A>T
c.899-8409A>T (n.899-8409A>T)
c.1582T>A (p.Ser528Thr)
4g.55443831T>ACA439485255CLOCK,TMEM165c.1758A>T (p.Ser586=)
c.353-8408T>A
n.340A>T
c.409-8408T>A
c.899-8408T>A (n.899-8408T>A)
c.1581A>T (p.Ser527=)
 dbSNP gnomAD v3 gnomAD v4
4g.55443831T>CCA439485256CLOCK,TMEM165c.1758A>G (p.Ser586=)
c.353-8408T>C
n.340A>G
c.409-8408T>C
c.899-8408T>C (n.899-8408T>C)
c.1581A>G (p.Ser527=)
4g.55443831T>GCA439485257CLOCK,TMEM165c.1758A>C (p.Ser586=)
c.353-8408T>G
n.340A>C
c.409-8408T>G
c.899-8408T>G (n.899-8408T>G)
c.1581A>C (p.Ser527=)
4g.55443832G>ACA356916011CLOCK,TMEM165c.1757C>T (p.Ser586Leu)
c.353-8407G>A
n.339C>T
c.409-8407G>A
c.899-8407G>A (n.899-8407G>A)
c.1580C>T (p.Ser527Leu)
4g.55443832G>CCA356916018CLOCK,TMEM165c.1757C>G (p.Ser586Ter)
c.353-8407G>C
n.339C>G
c.409-8407G>C
c.899-8407G>C (n.899-8407G>C)
c.1580C>G (p.Ser527Ter)
4g.55443832G>TCA356916022CLOCK,TMEM165c.1757C>A (p.Ser586Ter)
c.353-8407G>T
n.339C>A
c.409-8407G>T
c.899-8407G>T (n.899-8407G>T)
c.1580C>A (p.Ser527Ter)
4g.55443833A>CCA356916029CLOCK,TMEM165c.1756T>G (p.Ser586Ala)
c.353-8406A>C
n.338T>G
c.409-8406A>C
c.899-8406A>C (n.899-8406A>C)
c.1579T>G (p.Ser527Ala)
4g.55443833A>GCA356916027CLOCK,TMEM165c.1756T>C (p.Ser586Pro)
c.353-8406A>G
n.338T>C
c.409-8406A>G
c.899-8406A>G (n.899-8406A>G)
c.1579T>C (p.Ser527Pro)
4g.55443833A>TCA356916028CLOCK,TMEM165c.1756T>A (p.Ser586Thr)
c.353-8406A>T
n.338T>A
c.409-8406A>T
c.899-8406A>T (n.899-8406A>T)
c.1579T>A (p.Ser527Thr)
4g.55443834A>CCA356916030CLOCK,TMEM165c.1755T>G (p.Asn585Lys)
c.353-8405A>C
n.337T>G
c.409-8405A>C
c.899-8405A>C (n.899-8405A>C)
c.1578T>G (p.Asn526Lys)
4g.55443834A>GCA439485258CLOCK,TMEM165c.1755T>C (p.Asn585=)
c.353-8405A>G
n.337T>C
c.409-8405A>G
c.899-8405A>G (n.899-8405A>G)
c.1578T>C (p.Asn526=)
4g.55443834A>TCA356916033CLOCK,TMEM165c.1755T>A (p.Asn585Lys)
c.353-8405A>T
n.337T>A
c.409-8405A>T
c.899-8405A>T (n.899-8405A>T)
c.1578T>A (p.Asn526Lys)
4g.55443835T>ACA356916037CLOCK,TMEM165c.1754A>T (p.Asn585Ile)
c.353-8404T>A
n.336A>T
c.409-8404T>A
c.899-8404T>A (n.899-8404T>A)
c.1577A>T (p.Asn526Ile)
4g.55443835T>CCA356916038CLOCK,TMEM165c.1754A>G (p.Asn585Ser)
c.353-8404T>C
n.336A>G
c.409-8404T>C
c.899-8404T>C (n.899-8404T>C)
c.1577A>G (p.Asn526Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443835T>GCA356916039CLOCK,TMEM165c.1754A>C (p.Asn585Thr)
c.353-8404T>G
n.336A>C
c.409-8404T>G
c.899-8404T>G (n.899-8404T>G)
c.1577A>C (p.Asn526Thr)
4g.55443835T=CA1459075248CLOCK,TMEM165c.1754A= (p.Asn585=)
c.353-8404T=
n.336A=
c.409-8404T=
c.899-8404T= (n.899-8404T=)
c.1577A= (p.Asn526=)
4g.55443836T>ACA356916044CLOCK,TMEM165c.1753A>T (p.Asn585Tyr)
c.353-8403T>A
n.335A>T
c.409-8403T>A
c.899-8403T>A (n.899-8403T>A)
c.1576A>T (p.Asn526Tyr)
4g.55443836T>CCA356916040CLOCK,TMEM165c.1753A>G (p.Asn585Asp)
c.353-8403T>C
n.335A>G
c.409-8403T>C
c.899-8403T>C (n.899-8403T>C)
c.1576A>G (p.Asn526Asp)
4g.55443836T>GCA356916042CLOCK,TMEM165c.1753A>C (p.Asn585His)
c.353-8403T>G
n.335A>C
c.409-8403T>G
c.899-8403T>G (n.899-8403T>G)
c.1576A>C (p.Asn526His)
4g.55443837T>ACA439485261CLOCK,TMEM165c.1752A>T (p.Gly584=)
c.353-8402T>A
n.334A>T
c.409-8402T>A
c.899-8402T>A (n.899-8402T>A)
c.1575A>T (p.Gly525=)
4g.55443837T>CCA439485263CLOCK,TMEM165c.1752A>G (p.Gly584=)
c.353-8402T>C
n.334A>G
c.409-8402T>C
c.899-8402T>C (n.899-8402T>C)
c.1575A>G (p.Gly525=)
4g.55443837T>GCA439485262CLOCK,TMEM165c.1752A>C (p.Gly584=)
c.353-8402T>G
n.334A>C
c.409-8402T>G
c.899-8402T>G (n.899-8402T>G)
c.1575A>C (p.Gly525=)
4g.55443838C>ACA356916054CLOCK,TMEM165c.1751G>T (p.Gly584Val)
c.353-8401C>A
n.333G>T
c.409-8401C>A
c.899-8401C>A (n.899-8401C>A)
c.1574G>T (p.Gly525Val)
4g.55443838C>GCA356916057CLOCK,TMEM165c.1751G>C (p.Gly584Ala)
c.353-8401C>G
n.333G>C
c.409-8401C>G
c.899-8401C>G (n.899-8401C>G)
c.1574G>C (p.Gly525Ala)
4g.55443838C>TCA356916060CLOCK,TMEM165c.1751G>A (p.Gly584Glu)
c.353-8401C>T
n.333G>A
c.409-8401C>T
c.899-8401C>T (n.899-8401C>T)
c.1574G>A (p.Gly525Glu)
4g.55443839C>ACA356916063CLOCK,TMEM165c.1750G>T (p.Gly584Ter)
c.353-8400C>A
n.332G>T
c.409-8400C>A
c.899-8400C>A (n.899-8400C>A)
c.1573G>T (p.Gly525Ter)
4g.55443839C>GCA356916069CLOCK,TMEM165c.1750G>C (p.Gly584Arg)
c.353-8400C>G
n.332G>C
c.409-8400C>G
c.899-8400C>G (n.899-8400C>G)
c.1573G>C (p.Gly525Arg)
4g.55443839C>TCA356916072CLOCK,TMEM165c.1750G>A (p.Gly584Arg)
c.353-8400C>T
n.332G>A
c.409-8400C>T
c.899-8400C>T (n.899-8400C>T)
c.1573G>A (p.Gly525Arg)
4g.55443840A>CCA439485264CLOCK,TMEM165c.1749T>G (p.Ser583=)
c.353-8399A>C
n.331T>G
c.409-8399A>C
c.899-8399A>C (n.899-8399A>C)
c.1572T>G (p.Ser524=)
4g.55443840A>GCA439485266CLOCK,TMEM165c.1749T>C (p.Ser583=)
c.353-8399A>G
n.331T>C
c.409-8399A>G
c.899-8399A>G (n.899-8399A>G)
c.1572T>C (p.Ser524=)
 gnomAD v4
4g.55443840A>TCA439485267CLOCK,TMEM165c.1749T>A (p.Ser583=)
c.353-8399A>T
n.331T>A
c.409-8399A>T
c.899-8399A>T (n.899-8399A>T)
c.1572T>A (p.Ser524=)
4g.55443841G>ACA356916080CLOCK,TMEM165c.1748C>T (p.Ser583Phe)
c.353-8398G>A
n.330C>T
c.409-8398G>A
c.899-8398G>A (n.899-8398G>A)
c.1571C>T (p.Ser524Phe)
4g.55443841G>CCA356916081CLOCK,TMEM165c.1748C>G (p.Ser583Cys)
c.353-8398G>C
n.330C>G
c.409-8398G>C
c.899-8398G>C (n.899-8398G>C)
c.1571C>G (p.Ser524Cys)
4g.55443841G>TCA356916087CLOCK,TMEM165c.1748C>A (p.Ser583Tyr)
c.353-8398G>T
n.330C>A
c.409-8398G>T
c.899-8398G>T (n.899-8398G>T)
c.1571C>A (p.Ser524Tyr)
4g.55443842A=CA1459075252CLOCK,TMEM165c.1747T= (p.Ser583=)
c.353-8397A=
n.329T=
c.409-8397A=
c.899-8397A= (n.899-8397A=)
c.1570T= (p.Ser524=)
4g.55443842A>CCA2925819CLOCK,TMEM165c.1747T>G (p.Ser583Ala)
c.353-8397A>C
n.329T>G
c.409-8397A>C
c.899-8397A>C (n.899-8397A>C)
c.1570T>G (p.Ser524Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443842A>GCA356916094CLOCK,TMEM165c.1747T>C (p.Ser583Pro)
c.353-8397A>G
n.329T>C
c.409-8397A>G
c.899-8397A>G (n.899-8397A>G)
c.1570T>C (p.Ser524Pro)
4g.55443842A>TCA356916097CLOCK,TMEM165c.1747T>A (p.Ser583Thr)
c.353-8397A>T
n.329T>A
c.409-8397A>T
c.899-8397A>T (n.899-8397A>T)
c.1570T>A (p.Ser524Thr)
4g.55443843A>CCA439485268CLOCK,TMEM165c.1746T>G (p.Ser582=)
c.353-8396A>C
n.328T>G
c.409-8396A>C
c.899-8396A>C (n.899-8396A>C)
c.1569T>G (p.Ser523=)
 gnomAD v4
4g.55443843A>GCA439485270CLOCK,TMEM165c.1746T>C (p.Ser582=)
c.353-8396A>G
n.328T>C
c.409-8396A>G
c.899-8396A>G (n.899-8396A>G)
c.1569T>C (p.Ser523=)
 dbSNP gnomAD v4
4g.55443843A>TCA439485269CLOCK,TMEM165c.1746T>A (p.Ser582=)
c.353-8396A>T
n.328T>A
c.409-8396A>T
c.899-8396A>T (n.899-8396A>T)
c.1569T>A (p.Ser523=)
4g.55443844G>ACA356916099CLOCK,TMEM165c.1745C>T (p.Ser582Phe)
c.353-8395G>A
n.327C>T
c.409-8395G>A
c.899-8395G>A (n.899-8395G>A)
c.1568C>T (p.Ser523Phe)
4g.55443844G>CCA356916111CLOCK,TMEM165c.1745C>G (p.Ser582Cys)
c.353-8395G>C
n.327C>G
c.409-8395G>C
c.899-8395G>C (n.899-8395G>C)
c.1568C>G (p.Ser523Cys)
4g.55443844G>TCA356916103CLOCK,TMEM165c.1745C>A (p.Ser582Tyr)
c.353-8395G>T
n.327C>A
c.409-8395G>T
c.899-8395G>T (n.899-8395G>T)
c.1568C>A (p.Ser523Tyr)
 gnomAD v4
4g.55443845A>CCA356916115CLOCK,TMEM165c.1744T>G (p.Ser582Ala)
c.353-8394A>C
n.326T>G
c.409-8394A>C
c.899-8394A>C (n.899-8394A>C)
c.1567T>G (p.Ser523Ala)
4g.55443845A>GCA356916124CLOCK,TMEM165c.1744T>C (p.Ser582Pro)
c.353-8394A>G
n.326T>C
c.409-8394A>G
c.899-8394A>G (n.899-8394A>G)
c.1567T>C (p.Ser523Pro)
4g.55443845A>TCA356916119CLOCK,TMEM165c.1744T>A (p.Ser582Thr)
c.353-8394A>T
n.326T>A
c.409-8394A>T
c.899-8394A>T (n.899-8394A>T)
c.1567T>A (p.Ser523Thr)
4g.55443847delCA2670687918CLOCK,TMEM165c.1744del (p.Ser582LeufsTer14)
c.353-8392del
n.326del
c.409-8392del
c.899-8392del (n.899-8392del)
c.1567del (p.Ser523LeufsTer14)
 gnomAD v4
4g.55443846A>CCA439485274CLOCK,TMEM165c.1743T>G (p.Leu581=)
c.353-8393A>C
n.325T>G
c.409-8393A>C
c.899-8393A>C (n.899-8393A>C)
c.1566T>G (p.Leu522=)
 gnomAD v4
4g.55443846A>GCA439485275CLOCK,TMEM165c.1743T>C (p.Leu581=)
c.353-8393A>G
n.325T>C
c.409-8393A>G
c.899-8393A>G (n.899-8393A>G)
c.1566T>C (p.Leu522=)
4g.55443846A>TCA439485276CLOCK,TMEM165c.1743T>A (p.Leu581=)
c.353-8393A>T
n.325T>A
c.409-8393A>T
c.899-8393A>T (n.899-8393A>T)
c.1566T>A (p.Leu522=)
4g.55443847A>CCA356916130CLOCK,TMEM165c.1742T>G (p.Leu581Arg)
c.353-8392A>C
n.324T>G
c.409-8392A>C
c.899-8392A>C (n.899-8392A>C)
c.1565T>G (p.Leu522Arg)
4g.55443847A>GCA356916134CLOCK,TMEM165c.1742T>C (p.Leu581Pro)
c.353-8392A>G
n.324T>C
c.409-8392A>G
c.899-8392A>G (n.899-8392A>G)
c.1565T>C (p.Leu522Pro)
4g.55443847A>TCA356916135CLOCK,TMEM165c.1742T>A (p.Leu581His)
c.353-8392A>T
n.324T>A
c.409-8392A>T
c.899-8392A>T (n.899-8392A>T)
c.1565T>A (p.Leu522His)
4g.55443848G>ACA2925820CLOCK,TMEM165c.1741C>T (p.Leu581Phe)
c.353-8391G>A
n.323C>T
c.409-8391G>A
c.899-8391G>A (n.899-8391G>A)
c.1564C>T (p.Leu522Phe)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443848G>CCA356916136CLOCK,TMEM165c.1741C>G (p.Leu581Val)
c.353-8391G>C
n.323C>G
c.409-8391G>C
c.899-8391G>C (n.899-8391G>C)
c.1564C>G (p.Leu522Val)
 gnomAD v4
4g.55443848G=CA1459075255CLOCK,TMEM165c.1741C= (p.Leu581=)
c.353-8391G=
n.323C=
c.409-8391G=
c.899-8391G= (n.899-8391G=)
c.1564C= (p.Leu522=)
4g.55443848G>TCA356916138CLOCK,TMEM165c.1741C>A (p.Leu581Ile)
c.353-8391G>T
n.323C>A
c.409-8391G>T
c.899-8391G>T (n.899-8391G>T)
c.1564C>A (p.Leu522Ile)
4g.55443849T>ACA356916141CLOCK,TMEM165c.1740A>T (p.Gln580His)
c.353-8390T>A
n.322A>T
c.409-8390T>A
c.899-8390T>A (n.899-8390T>A)
c.1563A>T (p.Gln521His)
4g.55443849T>CCA2925821CLOCK,TMEM165c.1740A>G (p.Gln580=)
c.353-8390T>C
n.322A>G
c.409-8390T>C
c.899-8390T>C (n.899-8390T>C)
c.1563A>G (p.Gln521=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443849T>GCA356916146CLOCK,TMEM165c.1740A>C (p.Gln580His)
c.353-8390T>G
n.322A>C
c.409-8390T>G
c.899-8390T>G (n.899-8390T>G)
c.1563A>C (p.Gln521His)
 gnomAD v4
4g.55443849T=CA1459075257CLOCK,TMEM165c.1740A= (p.Gln580=)
c.353-8390T=
n.322A=
c.409-8390T=
c.899-8390T= (n.899-8390T=)
c.1563A= (p.Gln521=)
4g.55443850T>ACA356916160CLOCK,TMEM165c.1739A>T (p.Gln580Leu)
c.353-8389T>A
n.321A>T
c.409-8389T>A
c.899-8389T>A (n.899-8389T>A)
c.1562A>T (p.Gln521Leu)
4g.55443850T>CCA356916169CLOCK,TMEM165c.1739A>G (p.Gln580Arg)
c.353-8389T>C
n.321A>G
c.409-8389T>C
c.899-8389T>C (n.899-8389T>C)
c.1562A>G (p.Gln521Arg)
 gnomAD v4
4g.55443850T>GCA356916171CLOCK,TMEM165c.1739A>C (p.Gln580Pro)
c.353-8389T>G
n.321A>C
c.409-8389T>G
c.899-8389T>G (n.899-8389T>G)
c.1562A>C (p.Gln521Pro)
4g.55443850_55443851insACA2761734805CLOCK,TMEM165c.1738_1739insT (p.Gln580LeufsTer9)
c.353-8389_353-8388insA
n.320_321insT
c.409-8389_409-8388insA
c.899-8389_899-8388insA (n.899-8389_899-8388insA)
c.1561_1562insT (p.Gln521LeufsTer9)
4g.55443851G>ACA356916177CLOCK,TMEM165c.1738C>T (p.Gln580Ter)
c.353-8388G>A
n.320C>T
c.409-8388G>A
c.899-8388G>A (n.899-8388G>A)
c.1561C>T (p.Gln521Ter)
4g.55443851G>CCA356916197CLOCK,TMEM165c.1738C>G (p.Gln580Glu)
c.353-8388G>C
n.320C>G
c.409-8388G>C
c.899-8388G>C (n.899-8388G>C)
c.1561C>G (p.Gln521Glu)
4g.55443851G>TCA356916180CLOCK,TMEM165c.1738C>A (p.Gln580Lys)
c.353-8388G>T
n.320C>A
c.409-8388G>T
c.899-8388G>T (n.899-8388G>T)
c.1561C>A (p.Gln521Lys)
 dbSNP gnomAD v3 gnomAD v4
4g.55443852A>CCA439485281CLOCK,TMEM165c.1737T>G (p.Val579=)
c.353-8387A>C
n.319T>G
c.409-8387A>C
c.899-8387A>C (n.899-8387A>C)
c.1560T>G (p.Val520=)
4g.55443852A>GCA439485279CLOCK,TMEM165c.1737T>C (p.Val579=)
c.353-8387A>G
n.319T>C
c.409-8387A>G
c.899-8387A>G (n.899-8387A>G)
c.1560T>C (p.Val520=)
4g.55443852A>TCA439485280CLOCK,TMEM165c.1737T>A (p.Val579=)
c.353-8387A>T
n.319T>A
c.409-8387A>T
c.899-8387A>T (n.899-8387A>T)
c.1560T>A (p.Val520=)
4g.55443853A>CCA356916202CLOCK,TMEM165c.1736T>G (p.Val579Gly)
c.353-8386A>C
n.318T>G
c.409-8386A>C
c.899-8386A>C (n.899-8386A>C)
c.1559T>G (p.Val520Gly)
4g.55443853A>GCA356916205CLOCK,TMEM165c.1736T>C (p.Val579Ala)
c.353-8386A>G
n.318T>C
c.409-8386A>G
c.899-8386A>G (n.899-8386A>G)
c.1559T>C (p.Val520Ala)
4g.55443853A>TCA356916209CLOCK,TMEM165c.1736T>A (p.Val579Asp)
c.353-8386A>T
n.318T>A
c.409-8386A>T
c.899-8386A>T (n.899-8386A>T)
c.1559T>A (p.Val520Asp)
4g.55443854C>ACA356916212CLOCK,TMEM165c.1735G>T (p.Val579Phe)
c.353-8385C>A
n.317G>T
c.409-8385C>A
c.899-8385C>A (n.899-8385C>A)
c.1558G>T (p.Val520Phe)
 dbSNP
4g.55443854C=CA1459075259CLOCK,TMEM165c.1735G= (p.Val579=)
c.353-8385C=
n.317G=
c.409-8385C=
c.899-8385C= (n.899-8385C=)
c.1558G= (p.Val520=)
4g.55443854C>GCA356916218CLOCK,TMEM165c.1735G>C (p.Val579Leu)
c.353-8385C>G
n.317G>C
c.409-8385C>G
c.899-8385C>G (n.899-8385C>G)
c.1558G>C (p.Val520Leu)
4g.55443854C>TCA356916227CLOCK,TMEM165c.1735G>A (p.Val579Ile)
c.353-8385C>T
n.317G>A
c.409-8385C>T
c.899-8385C>T (n.899-8385C>T)
c.1558G>A (p.Val520Ile)
 dbSNP gnomAD v2 gnomAD v4
4g.55443855G>ACA96904800CLOCK,TMEM165c.1734C>T (p.Ser578=)
c.353-8384G>A
n.316C>T
c.409-8384G>A
c.899-8384G>A (n.899-8384G>A)
c.1557C>T (p.Ser519=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443855G>CCA439485282CLOCK,TMEM165c.1734C>G (p.Ser578=)
c.353-8384G>C
n.316C>G
c.409-8384G>C
c.899-8384G>C (n.899-8384G>C)
c.1557C>G (p.Ser519=)
4g.55443855G=CA1459075262CLOCK,TMEM165c.1734C= (p.Ser578=)
c.353-8384G=
n.316C=
c.409-8384G=
c.899-8384G= (n.899-8384G=)
c.1557C= (p.Ser519=)
4g.55443855G>TCA439485283CLOCK,TMEM165c.1734C>A (p.Ser578=)
c.353-8384G>T
n.316C>A
c.409-8384G>T
c.899-8384G>T (n.899-8384G>T)
c.1557C>A (p.Ser519=)
4g.55443856G>ACA356916236CLOCK,TMEM165c.1733C>T (p.Ser578Phe)
c.353-8383G>A
n.315C>T
c.409-8383G>A
c.899-8383G>A (n.899-8383G>A)
c.1556C>T (p.Ser519Phe)
4g.55443856G>CCA356916239CLOCK,TMEM165c.1733C>G (p.Ser578Cys)
c.353-8383G>C
n.315C>G
c.409-8383G>C
c.899-8383G>C (n.899-8383G>C)
c.1556C>G (p.Ser519Cys)
4g.55443856G>TCA356916241CLOCK,TMEM165c.1733C>A (p.Ser578Tyr)
c.353-8383G>T
n.315C>A
c.409-8383G>T
c.899-8383G>T (n.899-8383G>T)
c.1556C>A (p.Ser519Tyr)
4g.55443857A>CCA356916254CLOCK,TMEM165c.1732T>G (p.Ser578Ala)
c.353-8382A>C
n.314T>G
c.409-8382A>C
c.899-8382A>C (n.899-8382A>C)
c.1555T>G (p.Ser519Ala)
4g.55443857A>GCA356916256CLOCK,TMEM165c.1732T>C (p.Ser578Pro)
c.353-8382A>G
n.314T>C
c.409-8382A>G
c.899-8382A>G (n.899-8382A>G)
c.1555T>C (p.Ser519Pro)
4g.55443857A>TCA356916246CLOCK,TMEM165c.1732T>A (p.Ser578Thr)
c.353-8382A>T
n.314T>A
c.409-8382A>T
c.899-8382A>T (n.899-8382A>T)
c.1555T>A (p.Ser519Thr)
4g.55443858A>CCA439485286CLOCK,TMEM165c.1731T>G (p.Gly577=)
c.353-8381A>C
n.313T>G
c.409-8381A>C
c.899-8381A>C (n.899-8381A>C)
c.1554T>G (p.Gly518=)
4g.55443858A>GCA439485285CLOCK,TMEM165c.1731T>C (p.Gly577=)
c.353-8381A>G
n.313T>C
c.409-8381A>G
c.899-8381A>G (n.899-8381A>G)
c.1554T>C (p.Gly518=)
4g.55443858A>TCA439485287CLOCK,TMEM165c.1731T>A (p.Gly577=)
c.353-8381A>T
n.313T>A
c.409-8381A>T
c.899-8381A>T (n.899-8381A>T)
c.1554T>A (p.Gly518=)
4g.55443859C>ACA356916259CLOCK,TMEM165c.1730G>T (p.Gly577Val)
c.353-8380C>A
n.312G>T
c.409-8380C>A
c.899-8380C>A (n.899-8380C>A)
c.1553G>T (p.Gly518Val)
4g.55443859C>GCA356916260CLOCK,TMEM165c.1730G>C (p.Gly577Ala)
c.353-8380C>G
n.312G>C
c.409-8380C>G
c.899-8380C>G (n.899-8380C>G)
c.1553G>C (p.Gly518Ala)
4g.55443859C>TCA356916263CLOCK,TMEM165c.1730G>A (p.Gly577Asp)
c.353-8380C>T
n.312G>A
c.409-8380C>T
c.899-8380C>T (n.899-8380C>T)
c.1553G>A (p.Gly518Asp)
4g.55443860C>ACA356916268CLOCK,TMEM165c.1729G>T (p.Gly577Cys)
c.353-8379C>A
n.311G>T
c.409-8379C>A
c.899-8379C>A (n.899-8379C>A)
c.1552G>T (p.Gly518Cys)
4g.55443860C>GCA356916283CLOCK,TMEM165c.1729G>C (p.Gly577Arg)
c.353-8379C>G
n.311G>C
c.409-8379C>G
c.899-8379C>G (n.899-8379C>G)
c.1552G>C (p.Gly518Arg)
4g.55443860C>TCA356916289CLOCK,TMEM165c.1729G>A (p.Gly577Ser)
c.353-8379C>T
n.311G>A
c.409-8379C>T
c.899-8379C>T (n.899-8379C>T)
c.1552G>A (p.Gly518Ser)
4g.55443861A>CCA356916293CLOCK,TMEM165c.1728T>G (p.Phe576Leu)
c.353-8378A>C
n.310T>G
c.409-8378A>C
c.899-8378A>C (n.899-8378A>C)
c.1551T>G (p.Phe517Leu)
4g.55443861A>GCA439485288CLOCK,TMEM165c.1728T>C (p.Phe576=)
c.353-8378A>G
n.310T>C
c.409-8378A>G
c.899-8378A>G (n.899-8378A>G)
c.1551T>C (p.Phe517=)
4g.55443861A>TCA356916296CLOCK,TMEM165c.1728T>A (p.Phe576Leu)
c.353-8378A>T
n.310T>A
c.409-8378A>T
c.899-8378A>T (n.899-8378A>T)
c.1551T>A (p.Phe517Leu)
4g.55443862A>CCA356916300CLOCK,TMEM165c.1727T>G (p.Phe576Cys)
c.353-8377A>C
n.309T>G
c.409-8377A>C
c.899-8377A>C (n.899-8377A>C)
c.1550T>G (p.Phe517Cys)
4g.55443862A>GCA356916301CLOCK,TMEM165c.1727T>C (p.Phe576Ser)
c.353-8377A>G
n.309T>C
c.409-8377A>G
c.899-8377A>G (n.899-8377A>G)
c.1550T>C (p.Phe517Ser)
4g.55443862A>TCA356916302CLOCK,TMEM165c.1727T>A (p.Phe576Tyr)
c.353-8377A>T
n.309T>A
c.409-8377A>T
c.899-8377A>T (n.899-8377A>T)
c.1550T>A (p.Phe517Tyr)
4g.55443863A>CCA356916303CLOCK,TMEM165c.1726T>G (p.Phe576Val)
c.353-8376A>C
n.308T>G
c.409-8376A>C
c.899-8376A>C (n.899-8376A>C)
c.1549T>G (p.Phe517Val)
4g.55443863A>GCA356916304CLOCK,TMEM165c.1726T>C (p.Phe576Leu)
c.353-8376A>G
n.308T>C
c.409-8376A>G
c.899-8376A>G (n.899-8376A>G)
c.1549T>C (p.Phe517Leu)
4g.55443863A>TCA356916305CLOCK,TMEM165c.1726T>A (p.Phe576Ile)
c.353-8376A>T
n.308T>A
c.409-8376A>T
c.899-8376A>T (n.899-8376A>T)
c.1549T>A (p.Phe517Ile)
4g.55443863_55443864insCACCA2761734806CLOCK,TMEM165c.1725_1726insGTG (p.Asn575_Phe576insVal)
c.353-8376_353-8375insCAC
n.307_308insGTG
c.409-8376_409-8375insCAC
c.899-8376_899-8375insCAC (n.899-8376_899-8375insCAC)
c.1548_1549insGTG (p.Asn516_Phe517insVal)
4g.55443864A=CA1459075265CLOCK,TMEM165c.1725T= (p.Asn575=)
c.353-8375A=
n.307T=
c.409-8375A=
c.899-8375A= (n.899-8375A=)
c.1548T= (p.Asn516=)
4g.55443864A>CCA356916308CLOCK,TMEM165c.1725T>G (p.Asn575Lys)
c.353-8375A>C
n.307T>G
c.409-8375A>C
c.899-8375A>C (n.899-8375A>C)
c.1548T>G (p.Asn516Lys)
4g.55443864A>GCA96904804CLOCK,TMEM165c.1725T>C (p.Asn575=)
c.353-8375A>G
n.307T>C
c.409-8375A>G
c.899-8375A>G (n.899-8375A>G)
c.1548T>C (p.Asn516=)
 dbSNP gnomAD v3 gnomAD v4
4g.55443864A>TCA356916312CLOCK,TMEM165c.1725T>A (p.Asn575Lys)
c.353-8375A>T
n.307T>A
c.409-8375A>T
c.899-8375A>T (n.899-8375A>T)
c.1548T>A (p.Asn516Lys)
 dbSNP
4g.55443865T>ACA356916313CLOCK,TMEM165c.1724A>T (p.Asn575Ile)
c.353-8374T>A
n.306A>T
c.409-8374T>A
c.899-8374T>A (n.899-8374T>A)
c.1547A>T (p.Asn516Ile)
4g.55443865T>CCA356916318CLOCK,TMEM165c.1724A>G (p.Asn575Ser)
c.353-8374T>C
n.306A>G
c.409-8374T>C
c.899-8374T>C (n.899-8374T>C)
c.1547A>G (p.Asn516Ser)
 gnomAD v4
4g.55443865T>GCA356916320CLOCK,TMEM165c.1724A>C (p.Asn575Thr)
c.353-8374T>G
n.306A>C
c.409-8374T>G
c.899-8374T>G (n.899-8374T>G)
c.1547A>C (p.Asn516Thr)
4g.55443866T>ACA356916324CLOCK,TMEM165c.1723A>T (p.Asn575Tyr)
c.353-8373T>A
n.305A>T
c.409-8373T>A
c.899-8373T>A (n.899-8373T>A)
c.1546A>T (p.Asn516Tyr)
 dbSNP
4g.55443866T>CCA356916325CLOCK,TMEM165c.1723A>G (p.Asn575Asp)
c.353-8373T>C
n.305A>G
c.409-8373T>C
c.899-8373T>C (n.899-8373T>C)
c.1546A>G (p.Asn516Asp)
4g.55443866T>GCA356916326CLOCK,TMEM165c.1723A>C (p.Asn575His)
c.353-8373T>G
n.305A>C
c.409-8373T>G
c.899-8373T>G (n.899-8373T>G)
c.1546A>C (p.Asn516His)
4g.55443866T=CA1459075272CLOCK,TMEM165c.1723A= (p.Asn575=)
c.353-8373T=
n.305A=
c.409-8373T=
c.899-8373T= (n.899-8373T=)
c.1546A= (p.Asn516=)
4g.55443866_55443867insACA796425188CLOCK,TMEM165c.1722_1723insT (p.Asn575Ter)
c.353-8373_353-8372insA
n.304_305insT
c.409-8373_409-8372insA
c.899-8373_899-8372insA (n.899-8373_899-8372insA)
c.1545_1546insT (p.Asn516Ter)
 dbSNP
4g.55443867C>ACA356916327CLOCK,TMEM165c.1722G>T (p.Leu574Phe)
c.353-8372C>A
n.304G>T
c.409-8372C>A
c.899-8372C>A (n.899-8372C>A)
c.1545G>T (p.Leu515Phe)
 gnomAD v4
4g.55443867C=CA1459075277CLOCK,TMEM165c.1722G= (p.Leu574=)
c.353-8372C=
n.304G=
c.409-8372C=
c.899-8372C= (n.899-8372C=)
c.1545G= (p.Leu515=)
4g.55443867C>GCA356916328CLOCK,TMEM165c.1722G>C (p.Leu574Phe)
c.353-8372C>G
n.304G>C
c.409-8372C>G
c.899-8372C>G (n.899-8372C>G)
c.1545G>C (p.Leu515Phe)
4g.55443867C>TCA96904809CLOCK,TMEM165c.1722G>A (p.Leu574=)
c.353-8372C>T
n.304G>A
c.409-8372C>T
c.899-8372C>T (n.899-8372C>T)
c.1545G>A (p.Leu515=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443868A>CCA356916331CLOCK,TMEM165c.1721T>G (p.Leu574Trp)
c.353-8371A>C
n.303T>G
c.409-8371A>C
c.899-8371A>C (n.899-8371A>C)
c.1544T>G (p.Leu515Trp)
4g.55443868A>GCA356916335CLOCK,TMEM165c.1721T>C (p.Leu574Ser)
c.353-8371A>G
n.303T>C
c.409-8371A>G
c.899-8371A>G (n.899-8371A>G)
c.1544T>C (p.Leu515Ser)
4g.55443868A>TCA356916337CLOCK,TMEM165c.1721T>A (p.Leu574Ter)
c.353-8371A>T
n.303T>A
c.409-8371A>T
c.899-8371A>T (n.899-8371A>T)
c.1544T>A (p.Leu515Ter)
4g.55443869A>CCA356916341CLOCK,TMEM165c.1720T>G (p.Leu574Val)
c.353-8370A>C
n.302T>G
c.409-8370A>C
c.899-8370A>C (n.899-8370A>C)
c.1543T>G (p.Leu515Val)
4g.55443869A>GCA439485293CLOCK,TMEM165c.1720T>C (p.Leu574=)
c.353-8370A>G
n.302T>C
c.409-8370A>G
c.899-8370A>G (n.899-8370A>G)
c.1543T>C (p.Leu515=)
 gnomAD v4
4g.55443869A>TCA356916344CLOCK,TMEM165c.1720T>A (p.Leu574Met)
c.353-8370A>T
n.302T>A
c.409-8370A>T
c.899-8370A>T (n.899-8370A>T)
c.1543T>A (p.Leu515Met)
4g.55443869_55443871delinsACCCA1459075279CLOCK,TMEM165c.1718_1720delinsGGT (p.Gly573=)
c.353-8370_353-8368delinsACC
n.300_302delinsGGT
c.409-8370_409-8368delinsACC
c.899-8370_899-8368delinsACC (n.899-8370_899-8368delinsACC)
c.1541_1543delinsGGT (p.Gly514=)
4g.55443870C>ACA439485294CLOCK,TMEM165c.1719G>T (p.Gly573=)
c.353-8369C>A
n.301G>T
c.409-8369C>A
c.899-8369C>A (n.899-8369C>A)
c.1542G>T (p.Gly514=)
4g.55443870C=CA1459075281CLOCK,TMEM165c.1719G= (p.Gly573=)
c.353-8369C=
n.301G=
c.409-8369C=
c.899-8369C= (n.899-8369C=)
c.1542G= (p.Gly514=)
4g.55443870C>GCA439485295CLOCK,TMEM165c.1719G>C (p.Gly573=)
c.353-8369C>G
n.301G>C
c.409-8369C>G
c.899-8369C>G (n.899-8369C>G)
c.1542G>C (p.Gly514=)
4g.55443870C>TCA439485296CLOCK,TMEM165c.1719G>A (p.Gly573=)
c.353-8369C>T
n.301G>A
c.409-8369C>T
c.899-8369C>T (n.899-8369C>T)
c.1542G>A (p.Gly514=)
 dbSNP gnomAD v4
4g.55443871_55443872delCA551651889CLOCK,TMEM165c.1718_1719del (p.Gly573ValfsTer15)
c.353-8368_353-8367del
n.300_301del
c.409-8368_409-8367del
c.899-8368_899-8367del (n.899-8368_899-8367del)
c.1541_1542del (p.Gly514ValfsTer15)
 dbSNP gnomAD v2
4g.55443871C>ACA356916351CLOCK,TMEM165c.1718G>T (p.Gly573Val)
c.353-8368C>A
n.300G>T
c.409-8368C>A
c.899-8368C>A (n.899-8368C>A)
c.1541G>T (p.Gly514Val)
 gnomAD v4
4g.55443871C>GCA356916352CLOCK,TMEM165c.1718G>C (p.Gly573Ala)
c.353-8368C>G
n.300G>C
c.409-8368C>G
c.899-8368C>G (n.899-8368C>G)
c.1541G>C (p.Gly514Ala)
4g.55443871C>TCA356916349CLOCK,TMEM165c.1718G>A (p.Gly573Glu)
c.353-8368C>T
n.300G>A
c.409-8368C>T
c.899-8368C>T (n.899-8368C>T)
c.1541G>A (p.Gly514Glu)
 gnomAD v4
4g.55443872C>ACA356916354CLOCK,TMEM165c.1717G>T (p.Gly573Trp)
c.353-8367C>A
n.299G>T
c.409-8367C>A
c.899-8367C>A (n.899-8367C>A)
c.1540G>T (p.Gly514Trp)
4g.55443872C=CA1459075285CLOCK,TMEM165c.1717G= (p.Gly573=)
c.353-8367C=
n.299G=
c.409-8367C=
c.899-8367C= (n.899-8367C=)
c.1540G= (p.Gly514=)
4g.55443872C>GCA356916353CLOCK,TMEM165c.1717G>C (p.Gly573Arg)
c.353-8367C>G
n.299G>C
c.409-8367C>G
c.899-8367C>G (n.899-8367C>G)
c.1540G>C (p.Gly514Arg)
4g.55443872C>TCA356916356CLOCK,TMEM165c.1717G>A (p.Gly573Arg)
c.353-8367C>T
n.299G>A
c.409-8367C>T
c.899-8367C>T (n.899-8367C>T)
c.1540G>A (p.Gly514Arg)
 dbSNP gnomAD v2
4g.55443873A>CCA439485302CLOCK,TMEM165c.1716T>G (p.Pro572=)
c.353-8366A>C
n.298T>G
c.409-8366A>C
c.899-8366A>C (n.899-8366A>C)
c.1539T>G (p.Pro513=)
4g.55443873A>GCA439485301CLOCK,TMEM165c.1716T>C (p.Pro572=)
c.353-8366A>G
n.298T>C
c.409-8366A>G
c.899-8366A>G (n.899-8366A>G)
c.1539T>C (p.Pro513=)
4g.55443873A>TCA439485300CLOCK,TMEM165c.1716T>A (p.Pro572=)
c.353-8366A>T
n.298T>A
c.409-8366A>T
c.899-8366A>T (n.899-8366A>T)
c.1539T>A (p.Pro513=)
4g.55443873_55443874insAACA2670687919CLOCK,TMEM165c.1716_1717insTT (p.Gly573LeufsTer3)
c.353-8366_353-8365insAA
n.298_299insTT
c.409-8366_409-8365insAA
c.899-8366_899-8365insAA (n.899-8366_899-8365insAA)
c.1539_1540insTT (p.Gly514LeufsTer3)
 gnomAD v4
4g.55443874G>ACA356916367CLOCK,TMEM165c.1715C>T (p.Pro572Leu)
c.353-8365G>A
n.297C>T
c.409-8365G>A
c.899-8365G>A (n.899-8365G>A)
c.1538C>T (p.Pro513Leu)
4g.55443874G>CCA356916375CLOCK,TMEM165c.1715C>G (p.Pro572Arg)
c.353-8365G>C
n.297C>G
c.409-8365G>C
c.899-8365G>C (n.899-8365G>C)
c.1538C>G (p.Pro513Arg)
4g.55443874G>TCA356916373CLOCK,TMEM165c.1715C>A (p.Pro572His)
c.353-8365G>T
n.297C>A
c.409-8365G>T
c.899-8365G>T (n.899-8365G>T)
c.1538C>A (p.Pro513His)
4g.55443874_55443875insATCA2670687920CLOCK,TMEM165c.1714_1715insAT (p.Pro572HisfsTer4)
c.353-8365_353-8364insAT
n.296_297insAT
c.409-8365_409-8364insAT
c.899-8365_899-8364insAT (n.899-8365_899-8364insAT)
c.1537_1538insAT (p.Pro513HisfsTer4)
 gnomAD v4
4g.55443875G>ACA356916379CLOCK,TMEM165c.1714C>T (p.Pro572Ser)
c.353-8364G>A
n.296C>T
c.409-8364G>A
c.899-8364G>A (n.899-8364G>A)
c.1537C>T (p.Pro513Ser)
 COSMIC
4g.55443875G>CCA356916383CLOCK,TMEM165c.1714C>G (p.Pro572Ala)
c.353-8364G>C
n.296C>G
c.409-8364G>C
c.899-8364G>C (n.899-8364G>C)
c.1537C>G (p.Pro513Ala)
4g.55443875G=CA1459075287CLOCK,TMEM165c.1714C= (p.Pro572=)
c.353-8364G=
n.296C=
c.409-8364G=
c.899-8364G= (n.899-8364G=)
c.1537C= (p.Pro513=)
4g.55443875G>TCA356916380CLOCK,TMEM165c.1714C>A (p.Pro572Thr)
c.353-8364G>T
n.296C>A
c.409-8364G>T
c.899-8364G>T (n.899-8364G>T)
c.1537C>A (p.Pro513Thr)
 dbSNP gnomAD v2
4g.55443876A>CCA356916384CLOCK,TMEM165c.1713T>G (p.Asn571Lys)
c.353-8363A>C
n.295T>G
c.409-8363A>C
c.899-8363A>C (n.899-8363A>C)
c.1536T>G (p.Asn512Lys)
4g.55443876A>GCA439485303CLOCK,TMEM165c.1713T>C (p.Asn571=)
c.353-8363A>G
n.295T>C
c.409-8363A>G
c.899-8363A>G (n.899-8363A>G)
c.1536T>C (p.Asn512=)
4g.55443876A>TCA356916385CLOCK,TMEM165c.1713T>A (p.Asn571Lys)
c.353-8363A>T
n.295T>A
c.409-8363A>T
c.899-8363A>T (n.899-8363A>T)
c.1536T>A (p.Asn512Lys)
 gnomAD v4
4g.55443877T>ACA356916386CLOCK,TMEM165c.1712A>T (p.Asn571Ile)
c.353-8362T>A
n.294A>T
c.409-8362T>A
c.899-8362T>A (n.899-8362T>A)
c.1535A>T (p.Asn512Ile)
4g.55443877T>CCA356916388CLOCK,TMEM165c.1712A>G (p.Asn571Ser)
c.353-8362T>C
n.294A>G
c.409-8362T>C
c.899-8362T>C (n.899-8362T>C)
c.1535A>G (p.Asn512Ser)
4g.55443877T>GCA356916390CLOCK,TMEM165c.1712A>C (p.Asn571Thr)
c.353-8362T>G
n.294A>C
c.409-8362T>G
c.899-8362T>G (n.899-8362T>G)
c.1535A>C (p.Asn512Thr)
4g.55443878T>ACA356916392CLOCK,TMEM165c.1711A>T (p.Asn571Tyr)
c.353-8361T>A
n.293A>T
c.409-8361T>A
c.899-8361T>A (n.899-8361T>A)
c.1534A>T (p.Asn512Tyr)
4g.55443878T>CCA356916393CLOCK,TMEM165c.1711A>G (p.Asn571Asp)
c.353-8361T>C
n.293A>G
c.409-8361T>C
c.899-8361T>C (n.899-8361T>C)
c.1534A>G (p.Asn512Asp)
 gnomAD v4
4g.55443878T>GCA356916394CLOCK,TMEM165c.1711A>C (p.Asn571His)
c.353-8361T>G
n.293A>C
c.409-8361T>G
c.899-8361T>G (n.899-8361T>G)
c.1534A>C (p.Asn512His)
4g.55443879T>ACA439485305CLOCK,TMEM165c.1710A>T (p.Ser570=)
c.353-8360T>A
n.292A>T
c.409-8360T>A
c.899-8360T>A (n.899-8360T>A)
c.1533A>T (p.Ser511=)
4g.55443879T>CCA439485306CLOCK,TMEM165c.1710A>G (p.Ser570=)
c.353-8360T>C
n.292A>G
c.409-8360T>C
c.899-8360T>C (n.899-8360T>C)
c.1533A>G (p.Ser511=)
4g.55443879T>GCA439485307CLOCK,TMEM165c.1710A>C (p.Ser570=)
c.353-8360T>G
n.292A>C
c.409-8360T>G
c.899-8360T>G (n.899-8360T>G)
c.1533A>C (p.Ser511=)
4g.55443880G>ACA356916396CLOCK,TMEM165c.1709C>T (p.Ser570Leu)
c.353-8359G>A
n.291C>T
c.409-8359G>A
c.899-8359G>A (n.899-8359G>A)
c.1532C>T (p.Ser511Leu)
 dbSNP gnomAD v2 gnomAD v4
4g.55443880G>CCA356916399CLOCK,TMEM165c.1709C>G (p.Ser570Ter)
c.353-8359G>C
n.291C>G
c.409-8359G>C
c.899-8359G>C (n.899-8359G>C)
c.1532C>G (p.Ser511Ter)
 COSMIC
4g.55443880G=CA1459075289CLOCK,TMEM165c.1709C= (p.Ser570=)
c.353-8359G=
n.291C=
c.409-8359G=
c.899-8359G= (n.899-8359G=)
c.1532C= (p.Ser511=)
4g.55443880G>TCA356916400CLOCK,TMEM165c.1709C>A (p.Ser570Ter)
c.353-8359G>T
n.291C>A
c.409-8359G>T
c.899-8359G>T (n.899-8359G>T)
c.1532C>A (p.Ser511Ter)
4g.55443881A=CA1459075294CLOCK,TMEM165c.1708T= (p.Ser570=)
c.353-8358A=
n.290T=
c.409-8358A=
c.899-8358A= (n.899-8358A=)
c.1531T= (p.Ser511=)
4g.55443881A>CCA356916402CLOCK,TMEM165c.1708T>G (p.Ser570Ala)
c.353-8358A>C
n.290T>G
c.409-8358A>C
c.899-8358A>C (n.899-8358A>C)
c.1531T>G (p.Ser511Ala)
4g.55443881A>GCA356916401CLOCK,TMEM165c.1708T>C (p.Ser570Pro)
c.353-8358A>G
n.290T>C
c.409-8358A>G
c.899-8358A>G (n.899-8358A>G)
c.1531T>C (p.Ser511Pro)
4g.55443881A>TCA2925822CLOCK,TMEM165c.1708T>A (p.Ser570Thr)
c.353-8358A>T
n.290T>A
c.409-8358A>T
c.899-8358A>T (n.899-8358A>T)
c.1531T>A (p.Ser511Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443882T>ACA356916403CLOCK,TMEM165c.1707A>T (p.Gln569His)
c.353-8357T>A
n.289A>T
c.409-8357T>A
c.899-8357T>A (n.899-8357T>A)
c.1530A>T (p.Gln510His)
4g.55443882T>CCA439485308CLOCK,TMEM165c.1707A>G (p.Gln569=)
c.353-8357T>C
n.289A>G
c.409-8357T>C
c.899-8357T>C (n.899-8357T>C)
c.1530A>G (p.Gln510=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443882T>GCA356916404CLOCK,TMEM165c.1707A>C (p.Gln569His)
c.353-8357T>G
n.289A>C
c.409-8357T>G
c.899-8357T>G (n.899-8357T>G)
c.1530A>C (p.Gln510His)
4g.55443882T=CA1459075297CLOCK,TMEM165c.1707A= (p.Gln569=)
c.353-8357T=
n.289A=
c.409-8357T=
c.899-8357T= (n.899-8357T=)
c.1530A= (p.Gln510=)
4g.55443883T>ACA356916407CLOCK,TMEM165c.1706A>T (p.Gln569Leu)
c.353-8356T>A
n.288A>T
c.409-8356T>A
c.899-8356T>A (n.899-8356T>A)
c.1529A>T (p.Gln510Leu)
 COSMIC
4g.55443883T>CCA2925823CLOCK,TMEM165c.1706A>G (p.Gln569Arg)
c.353-8356T>C
n.288A>G
c.409-8356T>C
c.899-8356T>C (n.899-8356T>C)
c.1529A>G (p.Gln510Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443883T>GCA356916410CLOCK,TMEM165c.1706A>C (p.Gln569Pro)
c.353-8356T>G
n.288A>C
c.409-8356T>G
c.899-8356T>G (n.899-8356T>G)
c.1529A>C (p.Gln510Pro)
 dbSNP gnomAD v4
4g.55443883T=CA1459075300CLOCK,TMEM165c.1706A= (p.Gln569=)
c.353-8356T=
n.288A=
c.409-8356T=
c.899-8356T= (n.899-8356T=)
c.1529A= (p.Gln510=)
4g.55443884G>ACA356916418CLOCK,TMEM165c.1705C>T (p.Gln569Ter)
c.353-8355G>A
n.287C>T
c.409-8355G>A
c.899-8355G>A (n.899-8355G>A)
c.1528C>T (p.Gln510Ter)
4g.55443884G>CCA356916419CLOCK,TMEM165c.1705C>G (p.Gln569Glu)
c.353-8355G>C
n.287C>G
c.409-8355G>C
c.899-8355G>C (n.899-8355G>C)
c.1528C>G (p.Gln510Glu)
4g.55443884G>TCA356916421CLOCK,TMEM165c.1705C>A (p.Gln569Lys)
c.353-8355G>T
n.287C>A
c.409-8355G>T
c.899-8355G>T (n.899-8355G>T)
c.1528C>A (p.Gln510Lys)
4g.55443885T>ACA356916424CLOCK,TMEM165c.1704A>T (p.Gln568His)
c.353-8354T>A
n.286A>T
c.409-8354T>A
c.899-8354T>A (n.899-8354T>A)
c.1527A>T (p.Gln509His)
4g.55443885T>CCA2925824CLOCK,TMEM165c.1704A>G (p.Gln568=)
c.353-8354T>C
n.286A>G
c.409-8354T>C
c.899-8354T>C (n.899-8354T>C)
c.1527A>G (p.Gln509=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443885T>GCA356916433CLOCK,TMEM165c.1704A>C (p.Gln568His)
c.353-8354T>G
n.286A>C
c.409-8354T>G
c.899-8354T>G (n.899-8354T>G)
c.1527A>C (p.Gln509His)
4g.55443885T=CA1459075303CLOCK,TMEM165c.1704A= (p.Gln568=)
c.353-8354T=
n.286A=
c.409-8354T=
c.899-8354T= (n.899-8354T=)
c.1527A= (p.Gln509=)
4g.55443886T>ACA356916438CLOCK,TMEM165c.1703A>T (p.Gln568Leu)
c.353-8353T>A
n.285A>T
c.409-8353T>A
c.899-8353T>A (n.899-8353T>A)
c.1526A>T (p.Gln509Leu)
4g.55443886T>CCA356916436CLOCK,TMEM165c.1703A>G (p.Gln568Arg)
c.353-8353T>C
n.285A>G
c.409-8353T>C
c.899-8353T>C (n.899-8353T>C)
c.1526A>G (p.Gln509Arg)
4g.55443886T>GCA356916434CLOCK,TMEM165c.1703A>C (p.Gln568Pro)
c.353-8353T>G
n.285A>C
c.409-8353T>G
c.899-8353T>G (n.899-8353T>G)
c.1526A>C (p.Gln509Pro)
4g.55443887G>ACA356916442CLOCK,TMEM165c.1702C>T (p.Gln568Ter)
c.353-8352G>A
n.284C>T
c.409-8352G>A
c.899-8352G>A (n.899-8352G>A)
c.1525C>T (p.Gln509Ter)
4g.55443887G>CCA356916444CLOCK,TMEM165c.1702C>G (p.Gln568Glu)
c.353-8352G>C
n.284C>G
c.409-8352G>C
c.899-8352G>C (n.899-8352G>C)
c.1525C>G (p.Gln509Glu)
4g.55443887G>TCA356916445CLOCK,TMEM165c.1702C>A (p.Gln568Lys)
c.353-8352G>T
n.284C>A
c.409-8352G>T
c.899-8352G>T (n.899-8352G>T)
c.1525C>A (p.Gln509Lys)
4g.55443888C>ACA356916448CLOCK,TMEM165c.1701G>T (p.Leu567Phe)
c.353-8351C>A
n.283G>T
c.409-8351C>A
c.899-8351C>A (n.899-8351C>A)
c.1524G>T (p.Leu508Phe)
4g.55443888C>GCA356916450CLOCK,TMEM165c.1701G>C (p.Leu567Phe)
c.353-8351C>G
n.283G>C
c.409-8351C>G
c.899-8351C>G (n.899-8351C>G)
c.1524G>C (p.Leu508Phe)
4g.55443888C>TCA439485313CLOCK,TMEM165c.1701G>A (p.Leu567=)
c.353-8351C>T
n.283G>A
c.409-8351C>T
c.899-8351C>T (n.899-8351C>T)
c.1524G>A (p.Leu508=)
4g.55443889A=CA1459075306CLOCK,TMEM165c.1700T= (p.Leu567=)
c.353-8350A=
n.282T=
c.409-8350A=
c.899-8350A= (n.899-8350A=)
c.1523T= (p.Leu508=)
4g.55443889A>CCA356916453CLOCK,TMEM165c.1700T>G (p.Leu567Trp)
c.353-8350A>C
n.282T>G
c.409-8350A>C
c.899-8350A>C (n.899-8350A>C)
c.1523T>G (p.Leu508Trp)
 gnomAD v4
4g.55443889A>GCA356916454CLOCK,TMEM165c.1700T>C (p.Leu567Ser)
c.353-8350A>G
n.282T>C
c.409-8350A>G
c.899-8350A>G (n.899-8350A>G)
c.1523T>C (p.Leu508Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443889A>TCA356916456CLOCK,TMEM165c.1700T>A (p.Leu567Ter)
c.353-8350A>T
n.282T>A
c.409-8350A>T
c.899-8350A>T (n.899-8350A>T)
c.1523T>A (p.Leu508Ter)
4g.55443890A>CCA356916458CLOCK,TMEM165c.1699T>G (p.Leu567Val)
c.353-8349A>C
n.281T>G
c.409-8349A>C
c.899-8349A>C (n.899-8349A>C)
c.1522T>G (p.Leu508Val)
4g.55443890A>GCA439485317CLOCK,TMEM165c.1699T>C (p.Leu567=)
c.353-8349A>G
n.281T>C
c.409-8349A>G
c.899-8349A>G (n.899-8349A>G)
c.1522T>C (p.Leu508=)
 gnomAD v4
4g.55443890A>TCA356916459CLOCK,TMEM165c.1699T>A (p.Leu567Met)
c.353-8349A>T
n.281T>A
c.409-8349A>T
c.899-8349A>T (n.899-8349A>T)
c.1522T>A (p.Leu508Met)
4g.55443891A>CCA356916461CLOCK,TMEM165c.1698T>G (p.Phe566Leu)
c.353-8348A>C
n.280T>G
c.409-8348A>C
c.899-8348A>C (n.899-8348A>C)
c.1521T>G (p.Phe507Leu)
4g.55443891A>GCA439485318CLOCK,TMEM165c.1698T>C (p.Phe566=)
c.353-8348A>G
n.280T>C
c.409-8348A>G
c.899-8348A>G (n.899-8348A>G)
c.1521T>C (p.Phe507=)
4g.55443891A>TCA356916463CLOCK,TMEM165c.1698T>A (p.Phe566Leu)
c.353-8348A>T
n.280T>A
c.409-8348A>T
c.899-8348A>T (n.899-8348A>T)
c.1521T>A (p.Phe507Leu)
4g.55443892A>CCA356916468CLOCK,TMEM165c.1697T>G (p.Phe566Cys)
c.353-8347A>C
n.279T>G
c.409-8347A>C
c.899-8347A>C (n.899-8347A>C)
c.1520T>G (p.Phe507Cys)
4g.55443892A>GCA356916466CLOCK,TMEM165c.1697T>C (p.Phe566Ser)
c.353-8347A>G
n.279T>C
c.409-8347A>G
c.899-8347A>G (n.899-8347A>G)
c.1520T>C (p.Phe507Ser)
4g.55443892A>TCA356916465CLOCK,TMEM165c.1697T>A (p.Phe566Tyr)
c.353-8347A>T
n.279T>A
c.409-8347A>T
c.899-8347A>T (n.899-8347A>T)
c.1520T>A (p.Phe507Tyr)
4g.55443893A>CCA356916478CLOCK,TMEM165c.1696T>G (p.Phe566Val)
c.353-8346A>C
n.278T>G
c.409-8346A>C
c.899-8346A>C (n.899-8346A>C)
c.1519T>G (p.Phe507Val)
4g.55443893A>GCA356916480CLOCK,TMEM165c.1696T>C (p.Phe566Leu)
c.353-8346A>G
n.278T>C
c.409-8346A>G
c.899-8346A>G (n.899-8346A>G)
c.1519T>C (p.Phe507Leu)
4g.55443893A>TCA356916482CLOCK,TMEM165c.1696T>A (p.Phe566Ile)
c.353-8346A>T
n.278T>A
c.409-8346A>T
c.899-8346A>T (n.899-8346A>T)
c.1519T>A (p.Phe507Ile)
4g.55443894C>ACA356916484CLOCK,TMEM165c.1695G>T (p.Met565Ile)
c.353-8345C>A
n.277G>T
c.409-8345C>A
c.899-8345C>A (n.899-8345C>A)
c.1518G>T (p.Met506Ile)
4g.55443894C=CA1459075308CLOCK,TMEM165c.1695G= (p.Met565=)
c.353-8345C=
n.277G=
c.409-8345C=
c.899-8345C= (n.899-8345C=)
c.1518G= (p.Met506=)
4g.55443894C>GCA356916485CLOCK,TMEM165c.1695G>C (p.Met565Ile)
c.353-8345C>G
n.277G>C
c.409-8345C>G
c.899-8345C>G (n.899-8345C>G)
c.1518G>C (p.Met506Ile)
4g.55443894C>TCA2925825CLOCK,TMEM165c.1695G>A (p.Met565Ile)
c.353-8345C>T
n.277G>A
c.409-8345C>T
c.899-8345C>T (n.899-8345C>T)
c.1518G>A (p.Met506Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443895A>CCA356916488CLOCK,TMEM165c.1694T>G (p.Met565Arg)
c.353-8344A>C
n.276T>G
c.409-8344A>C
c.899-8344A>C (n.899-8344A>C)
c.1517T>G (p.Met506Arg)
4g.55443895A>GCA356916499CLOCK,TMEM165c.1694T>C (p.Met565Thr)
c.353-8344A>G
n.276T>C
c.409-8344A>G
c.899-8344A>G (n.899-8344A>G)
c.1517T>C (p.Met506Thr)
4g.55443895A>TCA356916502CLOCK,TMEM165c.1694T>A (p.Met565Lys)
c.353-8344A>T
n.276T>A
c.409-8344A>T
c.899-8344A>T (n.899-8344A>T)
c.1517T>A (p.Met506Lys)
4g.55443896T>ACA356916506CLOCK,TMEM165c.1693A>T (p.Met565Leu)
c.353-8343T>A
n.275A>T
c.409-8343T>A
c.899-8343T>A (n.899-8343T>A)
c.1516A>T (p.Met506Leu)
4g.55443896T>CCA356916508CLOCK,TMEM165c.1693A>G (p.Met565Val)
c.353-8343T>C
n.275A>G
c.409-8343T>C
c.899-8343T>C (n.899-8343T>C)
c.1516A>G (p.Met506Val)
4g.55443896T>GCA356916516CLOCK,TMEM165c.1693A>C (p.Met565Leu)
c.353-8343T>G
n.275A>C
c.409-8343T>G
c.899-8343T>G (n.899-8343T>G)
c.1516A>C (p.Met506Leu)
4g.55443897C>ACA356916525CLOCK,TMEM165c.1693-1G>T (n.1693-1G>T)
c.353-8342C>A
n.275-1G>T
c.409-8342C>A
c.899-8342C>A (n.899-8342C>A)
c.1516-1G>T (n.1516-1G>T)
4g.55443897C>GCA356916523CLOCK,TMEM165c.1693-1G>C (n.1693-1G>C)
c.353-8342C>G
n.275-1G>C
c.409-8342C>G
c.899-8342C>G (n.899-8342C>G)
c.1516-1G>C (n.1516-1G>C)
4g.55443897C>TCA356916518CLOCK,TMEM165c.1693-1G>A (n.1693-1G>A)
c.353-8342C>T
n.275-1G>A
c.409-8342C>T
c.899-8342C>T (n.899-8342C>T)
c.1516-1G>A (n.1516-1G>A)
 gnomAD v4
4g.55443898T>ACA356916527CLOCK,TMEM165c.1693-2A>T (n.1693-2A>T)
c.353-8341T>A
n.275-2A>T
c.409-8341T>A
c.899-8341T>A (n.899-8341T>A)
c.1516-2A>T (n.1516-2A>T)
4g.55443898T>CCA356916533CLOCK,TMEM165c.1693-2A>G (n.1693-2A>G)
c.353-8341T>C
n.275-2A>G
c.409-8341T>C
c.899-8341T>C (n.899-8341T>C)
c.1516-2A>G (n.1516-2A>G)
4g.55443898T>GCA356916530CLOCK,TMEM165c.1693-2A>C (n.1693-2A>C)
c.353-8341T>G
n.275-2A>C
c.409-8341T>G
c.899-8341T>G (n.899-8341T>G)
c.1516-2A>C (n.1516-2A>C)
4g.55443900T>CCA2578091695CLOCK,TMEM165c.1693-4A>G (n.1693-4A>G)
c.353-8339T>C
n.275-4A>G
c.409-8339T>C
c.899-8339T>C (n.899-8339T>C)
c.1516-4A>G (n.1516-4A>G)
4g.55443900_55443901delinsTACA1459075310CLOCK,TMEM165c.1693-5_1693-4delinsTA (n.1693-5_1693-4delinsTA)
c.353-8339_353-8338delinsTA
n.275-5_275-4delinsTA
c.409-8339_409-8338delinsTA
c.899-8339_899-8338delinsTA (n.899-8339_899-8338delinsTA)
c.1516-5_1516-4delinsTA (n.1516-5_1516-4delinsTA)
4g.55443905delCA551651893CLOCK,TMEM165c.1693-5del (n.1693-5del)
c.353-8334del
n.275-5del
c.409-8334del
c.899-8334del (n.899-8334del)
c.1516-5del (n.1516-5del)
 dbSNP gnomAD v2 gnomAD v4
4g.55443902A>GCA2761734807CLOCK,TMEM165c.1693-6T>C (n.1693-6T>C)
c.353-8337A>G
n.275-6T>C
c.409-8337A>G
c.899-8337A>G (n.899-8337A>G)
c.1516-6T>C (n.1516-6T>C)
4g.55443903A>GCA645531122CLOCK,TMEM165c.1693-7T>C (n.1693-7T>C)
c.353-8336A>G
n.275-7T>C
c.409-8336A>G
c.899-8336A>G (n.899-8336A>G)
c.1516-7T>C (n.1516-7T>C)
 COSMIC
4g.55443906T>CCA1459075314CLOCK,TMEM165c.1693-10A>G (n.1693-10A>G)
c.353-8333T>C
n.275-10A>G
c.409-8333T>C
c.899-8333T>C (n.899-8333T>C)
c.1516-10A>G (n.1516-10A>G)
 dbSNP gnomAD v4
4g.55443906T>GCA2670687921CLOCK,TMEM165c.1693-10A>C (n.1693-10A>C)
c.353-8333T>G
n.275-10A>C
c.409-8333T>G
c.899-8333T>G (n.899-8333T>G)
c.1516-10A>C (n.1516-10A>C)
 gnomAD v4
4g.55443906T=CA1459075313CLOCK,TMEM165c.1693-10A= (n.1693-10A=)
c.353-8333T=
n.275-10A=
c.409-8333T=
c.899-8333T= (n.899-8333T=)
c.1516-10A= (n.1516-10A=)
4g.55443907A=CA1459075316CLOCK,TMEM165c.1693-11T= (n.1693-11T=)
c.353-8332A=
n.275-11T=
c.409-8332A=
c.899-8332A= (n.899-8332A=)
c.1516-11T= (n.1516-11T=)
4g.55443907A>TCA551651894CLOCK,TMEM165c.1693-11T>A (n.1693-11T>A)
c.353-8332A>T
n.275-11T>A
c.409-8332A>T
c.899-8332A>T (n.899-8332A>T)
c.1516-11T>A (n.1516-11T>A)
 dbSNP gnomAD v2
4g.55443908A>CCA2670687922CLOCK,TMEM165c.1693-12T>G (n.1693-12T>G)
c.353-8331A>C
n.275-12T>G
c.409-8331A>C
c.899-8331A>C (n.899-8331A>C)
c.1516-12T>G (n.1516-12T>G)
 gnomAD v4
4g.55443908A>TCA2578091696CLOCK,TMEM165c.1693-12T>A (n.1693-12T>A)
c.353-8331A>T
n.275-12T>A
c.409-8331A>T
c.899-8331A>T (n.899-8331A>T)
c.1516-12T>A (n.1516-12T>A)
4g.55443909A=CA1459075319CLOCK,TMEM165c.1693-13T= (n.1693-13T=)
c.353-8330A=
n.275-13T=
c.409-8330A=
c.899-8330A= (n.899-8330A=)
c.1516-13T= (n.1516-13T=)
4g.55443909A>GCA2925826CLOCK,TMEM165c.1693-13T>C (n.1693-13T>C)
c.353-8330A>G
n.275-13T>C
c.409-8330A>G
c.899-8330A>G (n.899-8330A>G)
c.1516-13T>C (n.1516-13T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443910G>CCA796425232CLOCK,TMEM165c.1693-14C>G (n.1693-14C>G)
c.353-8329G>C
n.275-14C>G
c.409-8329G>C
c.899-8329G>C (n.899-8329G>C)
c.1516-14C>G (n.1516-14C>G)
 dbSNP
4g.55443910G=CA1459075323CLOCK,TMEM165c.1693-14C= (n.1693-14C=)
c.353-8329G=
n.275-14C=
c.409-8329G=
c.899-8329G= (n.899-8329G=)
c.1516-14C= (n.1516-14C=)
4g.55443910_55443911delinsGACA1459075322CLOCK,TMEM165c.1693-15_1693-14delinsTC (n.1693-15_1693-14delinsTC)
c.353-8329_353-8328delinsGA
n.275-15_275-14delinsTC
c.409-8329_409-8328delinsGA
c.899-8329_899-8328delinsGA (n.899-8329_899-8328delinsGA)
c.1516-15_1516-14delinsTC (n.1516-15_1516-14delinsTC)
4g.55443910_55443911insCTCTACA551651895CLOCK,TMEM165c.1693-15_1693-14insTAGAG (n.1693-15_1693-14insTAGAG)
c.353-8329_353-8328insCTCTA
n.275-15_275-14insTAGAG
c.409-8329_409-8328insCTCTA
c.899-8329_899-8328insCTCTA (n.899-8329_899-8328insCTCTA)
c.1516-15_1516-14insTAGAG (n.1516-15_1516-14insTAGAG)
 dbSNP gnomAD v2
4g.55443911delCA1459075327CLOCK,TMEM165c.1693-15del (n.1693-15del)
c.353-8328del
n.275-15del
c.409-8328del
c.899-8328del (n.899-8328del)
c.1516-15del (n.1516-15del)
 dbSNP
4g.55443911A>GCA2670687923CLOCK,TMEM165c.1693-15T>C (n.1693-15T>C)
c.353-8328A>G
n.275-15T>C
c.409-8328A>G
c.899-8328A>G (n.899-8328A>G)
c.1516-15T>C (n.1516-15T>C)
 gnomAD v4
4g.55443913T>GCA796425233CLOCK,TMEM165c.1693-17A>C (n.1693-17A>C)
c.353-8326T>G
n.275-17A>C
c.409-8326T>G
c.899-8326T>G (n.899-8326T>G)
c.1516-17A>C (n.1516-17A>C)
 dbSNP gnomAD v3 gnomAD v4
4g.55443913T=CA1459075328CLOCK,TMEM165c.1693-17A= (n.1693-17A=)
c.353-8326T=
n.275-17A=
c.409-8326T=
c.899-8326T= (n.899-8326T=)
c.1516-17A= (n.1516-17A=)
4g.55443914_55443916delinsATGCA1459075330CLOCK,TMEM165c.1693-20_1693-18delinsCAT (n.1693-20_1693-18delinsCAT)
c.353-8325_353-8323delinsATG
n.275-20_275-18delinsCAT
c.409-8325_409-8323delinsATG
c.899-8325_899-8323delinsATG (n.899-8325_899-8323delinsATG)
c.1516-20_1516-18delinsCAT (n.1516-20_1516-18delinsCAT)
4g.55443915T>CCA2925828CLOCK,TMEM165c.1693-19A>G (n.1693-19A>G)
c.353-8324T>C
n.275-19A>G
c.409-8324T>C
c.899-8324T>C (n.899-8324T>C)
c.1516-19A>G (n.1516-19A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443915T=CA1459075332CLOCK,TMEM165c.1693-19A= (n.1693-19A=)
c.353-8324T=
n.275-19A=
c.409-8324T=
c.899-8324T= (n.899-8324T=)
c.1516-19A= (n.1516-19A=)
4g.55443916_55443917delCA2925827CLOCK,TMEM165c.1693-20_1693-19del (n.1693-20_1693-19del)
c.353-8323_353-8322del
n.275-20_275-19del
c.409-8323_409-8322del
c.899-8323_899-8322del (n.899-8323_899-8322del)
c.1516-20_1516-19del (n.1516-20_1516-19del)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443916G>TCA2670687924CLOCK,TMEM165c.1693-20C>A (n.1693-20C>A)
c.353-8323G>T
n.275-20C>A
c.409-8323G>T
c.899-8323G>T (n.899-8323G>T)
c.1516-20C>A (n.1516-20C>A)
 gnomAD v4
4g.55443918T>ACA2670687925CLOCK,TMEM165c.1693-22A>T (n.1693-22A>T)
c.353-8321T>A
n.275-22A>T
c.409-8321T>A
c.899-8321T>A (n.899-8321T>A)
c.1516-22A>T (n.1516-22A>T)
 gnomAD v4
4g.55443918T>GCA2598175393CLOCK,TMEM165c.1693-22A>C (n.1693-22A>C)
c.353-8321T>G
n.275-22A>C
c.409-8321T>G
c.899-8321T>G (n.899-8321T>G)
c.1516-22A>C (n.1516-22A>C)
 dbSNP gnomAD v3 gnomAD v4
4g.55443919A=CA1459075334CLOCK,TMEM165c.1693-23T= (n.1693-23T=)
c.353-8320A=
n.275-23T=
c.409-8320A=
c.899-8320A= (n.899-8320A=)
c.1516-23T= (n.1516-23T=)
4g.55443919A>GCA551651896CLOCK,TMEM165c.1693-23T>C (n.1693-23T>C)
c.353-8320A>G
n.275-23T>C
c.409-8320A>G
c.899-8320A>G (n.899-8320A>G)
c.1516-23T>C (n.1516-23T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443922A=CA1459075335CLOCK,TMEM165c.1693-26T= (n.1693-26T=)
c.353-8317A=
n.275-26T=
c.409-8317A=
c.899-8317A= (n.899-8317A=)
c.1516-26T= (n.1516-26T=)
4g.55443923T>GCA2670687926CLOCK,TMEM165c.1693-27A>C (n.1693-27A>C)
c.353-8316T>G
n.275-27A>C
c.409-8316T>G
c.899-8316T>G (n.899-8316T>G)
c.1516-27A>C (n.1516-27A>C)
 gnomAD v4
4g.55443923_55443924insTTCA551651897CLOCK,TMEM165c.1693-27_1693-26insAA (n.1693-27_1693-26insAA)
c.353-8316_353-8315insTT
n.275-27_275-26insAA
c.409-8316_409-8315insTT
c.899-8316_899-8315insTT (n.899-8316_899-8315insTT)
c.1516-27_1516-26insAA (n.1516-27_1516-26insAA)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443923_55443924delinsTGCA1459075337CLOCK,TMEM165c.1693-28_1693-27delinsCA (n.1693-28_1693-27delinsCA)
c.353-8316_353-8315delinsTG
n.275-28_275-27delinsCA
c.409-8316_409-8315delinsTG
c.899-8316_899-8315delinsTG (n.899-8316_899-8315delinsTG)
c.1516-28_1516-27delinsCA (n.1516-28_1516-27delinsCA)
4g.55443924delCA551651899CLOCK,TMEM165c.1693-28del (n.1693-28del)
c.353-8315del
n.275-28del
c.409-8315del
c.899-8315del (n.899-8315del)
c.1516-28del (n.1516-28del)
 dbSNP gnomAD v2
4g.55443924G>ACA551651898CLOCK,TMEM165c.1693-28C>T (n.1693-28C>T)
c.353-8315G>A
n.275-28C>T
c.409-8315G>A
c.899-8315G>A (n.899-8315G>A)
c.1516-28C>T (n.1516-28C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55443924G=CA1459075345CLOCK,TMEM165c.1693-28C= (n.1693-28C=)
c.353-8315G=
n.275-28C=
c.409-8315G=
c.899-8315G= (n.899-8315G=)
c.1516-28C= (n.1516-28C=)
4g.55443924G>TCA2925829CLOCK,TMEM165c.1693-28C>A (n.1693-28C>A)
c.353-8315G>T
n.275-28C>A
c.409-8315G>T
c.899-8315G>T (n.899-8315G>T)
c.1516-28C>A (n.1516-28C>A)
 dbSNP ExAC gnomAD v2
4g.55443926G>ACA2670687927CLOCK,TMEM165c.1693-30C>T (n.1693-30C>T)
c.353-8313G>A
n.275-30C>T
c.409-8313G>A
c.899-8313G>A (n.899-8313G>A)
c.1516-30C>T (n.1516-30C>T)
 gnomAD v4
4g.55443926G=CA1459075348CLOCK,TMEM165c.1693-30C= (n.1693-30C=)
c.353-8313G=
n.275-30C=
c.409-8313G=
c.899-8313G= (n.899-8313G=)
c.1516-30C= (n.1516-30C=)
4g.55443926G>TCA551651900CLOCK,TMEM165c.1693-30C>A (n.1693-30C>A)
c.353-8313G>T
n.275-30C>A
c.409-8313G>T
c.899-8313G>T (n.899-8313G>T)
c.1516-30C>A (n.1516-30C>A)
 dbSNP gnomAD v2
4g.55443927C>ACA2670687928CLOCK,TMEM165c.1693-31G>T (n.1693-31G>T)
c.353-8312C>A
n.275-31G>T
c.409-8312C>A
c.899-8312C>A (n.899-8312C>A)
c.1516-31G>T (n.1516-31G>T)
 gnomAD v4
4g.55443927C=CA1459075349CLOCK,TMEM165c.1693-31G= (n.1693-31G=)
c.353-8312C=
n.275-31G=
c.409-8312C=
c.899-8312C= (n.899-8312C=)
c.1516-31G= (n.1516-31G=)
4g.55443927C>GCA2670687929CLOCK,TMEM165c.1693-31G>C (n.1693-31G>C)
c.353-8312C>G
n.275-31G>C
c.409-8312C>G
c.899-8312C>G (n.899-8312C>G)
c.1516-31G>C (n.1516-31G>C)
 gnomAD v4
4g.55443927C>TCA2670687930CLOCK,TMEM165c.1693-31G>A (n.1693-31G>A)
c.353-8312C>T
n.275-31G>A
c.409-8312C>T
c.899-8312C>T (n.899-8312C>T)
c.1516-31G>A (n.1516-31G>A)
 gnomAD v4
4g.55443927_55443928insACA551651901CLOCK,TMEM165c.1693-32_1693-31insT (n.1693-32_1693-31insT)
c.353-8312_353-8311insA
n.275-32_275-31insT
c.409-8312_409-8311insA
c.899-8312_899-8311insA (n.899-8312_899-8311insA)
c.1516-32_1516-31insT (n.1516-32_1516-31insT)
 dbSNP gnomAD v2
4g.55443930delCA2505492412CLOCK,TMEM165c.1693-32del (n.1693-32del)
c.353-8309del
n.275-32del
c.409-8309del
c.899-8309del (n.899-8309del)
c.1516-32del (n.1516-32del)
 gnomAD v4

Number of alleles fetched