Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.95101794_95101797dupCA658822329AOPEP,FANCCn.410+21014_410+21017dup
n.2402_2405dup
c.1587_1590dup (p.Tyr531LeufsTer10)
c.1732_1735dup (n.1732_1735dup)
c.906_909dup (p.Tyr304LeufsTer10)
c.1422_1425dup (p.Tyr476LeufsTer10)
c.1131_1134dup (p.Tyr379LeufsTer10)
c.2319+21014_2319+21017dup (n.2319+21014_2319+21017dup)
c.966_969dup (p.Tyr324LeufsTer10)
 ClinVar dbSNP
9g.95101796A=CA1865459555AOPEP,FANCCn.410+21016A=
n.2403T=
c.1588T= (p.Leu530=)
c.1733T= (n.1733T=)
c.907T= (p.Leu303=)
c.1423T= (p.Leu475=)
c.1132T= (p.Leu378=)
c.2319+21016A= (n.2319+21016A=)
c.967T= (p.Leu323=)
9g.95101796A>CCA374104602AOPEP,FANCCn.410+21016A>C
n.2403T>G
c.1588T>G (p.Leu530Val)
c.1733T>G (n.1733T>G)
c.907T>G (p.Leu303Val)
c.1423T>G (p.Leu475Val)
c.1132T>G (p.Leu378Val)
c.2319+21016A>C (n.2319+21016A>C)
c.967T>G (p.Leu323Val)
9g.95101796A>GCA196536766AOPEP,FANCCn.410+21016A>G
n.2403T>C
c.1588T>C (p.Leu530=)
c.1733T>C (n.1733T>C)
c.907T>C (p.Leu303=)
c.1423T>C (p.Leu475=)
c.1132T>C (p.Leu378=)
c.2319+21016A>G (n.2319+21016A>G)
c.967T>C (p.Leu323=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.95101796A>TCA374104605AOPEP,FANCCn.410+21016A>T
n.2403T>A
c.1588T>A (p.Leu530Met)
c.1733T>A (n.1733T>A)
c.907T>A (p.Leu303Met)
c.1423T>A (p.Leu475Met)
c.1132T>A (p.Leu378Met)
c.2319+21016A>T (n.2319+21016A>T)
c.967T>A (p.Leu323Met)
9g.95101797G>ACA466092088AOPEP,FANCCn.410+21017G>A
n.2402C>T
c.1587C>T (p.Thr529=)
c.1732C>T (n.1732C>T)
c.906C>T (p.Thr302=)
c.1422C>T (p.Thr474=)
c.1131C>T (p.Thr377=)
c.2319+21017G>A (n.2319+21017G>A)
c.966C>T (p.Thr322=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.95101797G>CCA196536770AOPEP,FANCCn.410+21017G>C
n.2402C>G
c.1587C>G (p.Thr529=)
c.1732C>G (n.1732C>G)
c.906C>G (p.Thr302=)
c.1422C>G (p.Thr474=)
c.1131C>G (p.Thr377=)
c.2319+21017G>C (n.2319+21017G>C)
c.966C>G (p.Thr322=)
 ClinVar dbSNP gnomAD v4
9g.95101797G=CA1865459556AOPEP,FANCCn.410+21017G=
n.2402C=
c.1587C= (p.Thr529=)
c.1732C= (n.1732C=)
c.906C= (p.Thr302=)
c.1422C= (p.Thr474=)
c.1131C= (p.Thr377=)
c.2319+21017G= (n.2319+21017G=)
c.966C= (p.Thr322=)
9g.95101797G>TCA466092089AOPEP,FANCCn.410+21017G>T
n.2402C>A
c.1587C>A (p.Thr529=)
c.1732C>A (n.1732C>A)
c.906C>A (p.Thr302=)
c.1422C>A (p.Thr474=)
c.1131C>A (p.Thr377=)
c.2319+21017G>T (n.2319+21017G>T)
c.966C>A (p.Thr322=)
9g.95101798G>ACA374104607AOPEP,FANCCn.410+21018G>A
n.2401C>T
c.1586C>T (p.Thr529Ile)
c.1731C>T (n.1731C>T)
c.905C>T (p.Thr302Ile)
c.1421C>T (p.Thr474Ile)
c.1130C>T (p.Thr377Ile)
c.2319+21018G>A (n.2319+21018G>A)
c.965C>T (p.Thr322Ile)
9g.95101798G>CCA374104610AOPEP,FANCCn.410+21018G>C
n.2401C>G
c.1586C>G (p.Thr529Ser)
c.1731C>G (n.1731C>G)
c.905C>G (p.Thr302Ser)
c.1421C>G (p.Thr474Ser)
c.1130C>G (p.Thr377Ser)
c.2319+21018G>C (n.2319+21018G>C)
c.965C>G (p.Thr322Ser)
9g.95101798G>TCA374104612AOPEP,FANCCn.410+21018G>T
n.2401C>A
c.1586C>A (p.Thr529Asn)
c.1731C>A (n.1731C>A)
c.905C>A (p.Thr302Asn)
c.1421C>A (p.Thr474Asn)
c.1130C>A (p.Thr377Asn)
c.2319+21018G>T (n.2319+21018G>T)
c.965C>A (p.Thr322Asn)
 ClinVar gnomAD v4
9g.95101799T>ACA374104614AOPEP,FANCCn.410+21019T>A
n.2400A>T
c.1585A>T (p.Thr529Ser)
c.1730A>T (n.1730A>T)
c.904A>T (p.Thr302Ser)
c.1420A>T (p.Thr474Ser)
c.1129A>T (p.Thr377Ser)
c.2319+21019T>A (n.2319+21019T>A)
c.964A>T (p.Thr322Ser)
 ClinVar dbSNP
9g.95101799T>CCA374104616AOPEP,FANCCn.410+21019T>C
n.2400A>G
c.1585A>G (p.Thr529Ala)
c.1730A>G (n.1730A>G)
c.904A>G (p.Thr302Ala)
c.1420A>G (p.Thr474Ala)
c.1129A>G (p.Thr377Ala)
c.2319+21019T>C (n.2319+21019T>C)
c.964A>G (p.Thr322Ala)
9g.95101799T>GCA159396AOPEP,FANCCn.410+21019T>G
n.2400A>C
c.1585A>C (p.Thr529Pro)
c.1730A>C (n.1730A>C)
c.904A>C (p.Thr302Pro)
c.1420A>C (p.Thr474Pro)
c.1129A>C (p.Thr377Pro)
c.2319+21019T>G (n.2319+21019T>G)
c.964A>C (p.Thr322Pro)
 ClinVar dbSNP
9g.95101799T=CA1865459557AOPEP,FANCCn.410+21019T=
n.2400A=
c.1585A= (p.Thr529=)
c.1730A= (n.1730A=)
c.904A= (p.Thr302=)
c.1420A= (p.Thr474=)
c.1129A= (p.Thr377=)
c.2319+21019T= (n.2319+21019T=)
c.964A= (p.Thr322=)
9g.95101800C>ACA374104618AOPEP,FANCCn.410+21020C>A
n.2399G>T
c.1584G>T (p.Gln528His)
c.1729G>T (n.1729G>T)
c.903G>T (p.Gln301His)
c.1419G>T (p.Gln473His)
c.1128G>T (p.Gln376His)
c.2319+21020C>A (n.2319+21020C>A)
c.963G>T (p.Gln321His)
9g.95101800C>GCA374104619AOPEP,FANCCn.410+21020C>G
n.2399G>C
c.1584G>C (p.Gln528His)
c.1729G>C (n.1729G>C)
c.903G>C (p.Gln301His)
c.1419G>C (p.Gln473His)
c.1128G>C (p.Gln376His)
c.2319+21020C>G (n.2319+21020C>G)
c.963G>C (p.Gln321His)
9g.95101800C>TCA466092090AOPEP,FANCCn.410+21020C>T
n.2399G>A
c.1584G>A (p.Gln528=)
c.1729G>A (n.1729G>A)
c.903G>A (p.Gln301=)
c.1419G>A (p.Gln473=)
c.1128G>A (p.Gln376=)
c.2319+21020C>T (n.2319+21020C>T)
c.963G>A (p.Gln321=)
 ClinVar
9g.95101801T>ACA374104622AOPEP,FANCCn.410+21021T>A
n.2398A>T
c.1583A>T (p.Gln528Leu)
c.1728A>T (n.1728A>T)
c.902A>T (p.Gln301Leu)
c.1418A>T (p.Gln473Leu)
c.1127A>T (p.Gln376Leu)
c.2319+21021T>A (n.2319+21021T>A)
c.962A>T (p.Gln321Leu)
9g.95101801T>CCA374104624AOPEP,FANCCn.410+21021T>C
n.2398A>G
c.1583A>G (p.Gln528Arg)
c.1728A>G (n.1728A>G)
c.902A>G (p.Gln301Arg)
c.1418A>G (p.Gln473Arg)
c.1127A>G (p.Gln376Arg)
c.2319+21021T>C (n.2319+21021T>C)
c.962A>G (p.Gln321Arg)
9g.95101801T>GCA374104626AOPEP,FANCCn.410+21021T>G
n.2398A>C
c.1583A>C (p.Gln528Pro)
c.1728A>C (n.1728A>C)
c.902A>C (p.Gln301Pro)
c.1418A>C (p.Gln473Pro)
c.1127A>C (p.Gln376Pro)
c.2319+21021T>G (n.2319+21021T>G)
c.962A>C (p.Gln321Pro)
9g.95101802G>ACA374104629AOPEP,FANCCn.410+21022G>A
n.2397C>T
c.1582C>T (p.Gln528Ter)
c.1727C>T (n.1727C>T)
c.901C>T (p.Gln301Ter)
c.1417C>T (p.Gln473Ter)
c.1126C>T (p.Gln376Ter)
c.2319+21022G>A (n.2319+21022G>A)
c.961C>T (p.Gln321Ter)
 ClinVar
9g.95101802G>CCA374104631AOPEP,FANCCn.410+21022G>C
n.2397C>G
c.1582C>G (p.Gln528Glu)
c.1727C>G (n.1727C>G)
c.901C>G (p.Gln301Glu)
c.1417C>G (p.Gln473Glu)
c.1126C>G (p.Gln376Glu)
c.2319+21022G>C (n.2319+21022G>C)
c.961C>G (p.Gln321Glu)
9g.95101802G>TCA374104633AOPEP,FANCCn.410+21022G>T
n.2397C>A
c.1582C>A (p.Gln528Lys)
c.1727C>A (n.1727C>A)
c.901C>A (p.Gln301Lys)
c.1417C>A (p.Gln473Lys)
c.1126C>A (p.Gln376Lys)
c.2319+21022G>T (n.2319+21022G>T)
c.961C>A (p.Gln321Lys)
9g.95101803G>ACA466092091AOPEP,FANCCn.410+21023G>A
n.2396C>T
c.1581C>T (p.Asp527=)
c.1726C>T (n.1726C>T)
c.900C>T (p.Asp300=)
c.1416C>T (p.Asp472=)
c.1125C>T (p.Asp375=)
c.2319+21023G>A (n.2319+21023G>A)
c.960C>T (p.Asp320=)
9g.95101803G>CCA374104635AOPEP,FANCCn.410+21023G>C
n.2396C>G
c.1581C>G (p.Asp527Glu)
c.1726C>G (n.1726C>G)
c.900C>G (p.Asp300Glu)
c.1416C>G (p.Asp472Glu)
c.1125C>G (p.Asp375Glu)
c.2319+21023G>C (n.2319+21023G>C)
c.960C>G (p.Asp320Glu)
9g.95101803G>TCA374104637AOPEP,FANCCn.410+21023G>T
n.2396C>A
c.1581C>A (p.Asp527Glu)
c.1726C>A (n.1726C>A)
c.900C>A (p.Asp300Glu)
c.1416C>A (p.Asp472Glu)
c.1125C>A (p.Asp375Glu)
c.2319+21023G>T (n.2319+21023G>T)
c.960C>A (p.Asp320Glu)
9g.95101804T>ACA374104640AOPEP,FANCCn.410+21024T>A
n.2395A>T
c.1580A>T (p.Asp527Val)
c.1725A>T (n.1725A>T)
c.899A>T (p.Asp300Val)
c.1415A>T (p.Asp472Val)
c.1124A>T (p.Asp375Val)
c.2319+21024T>A (n.2319+21024T>A)
c.959A>T (p.Asp320Val)
 dbSNP
9g.95101804T>CCA374104642AOPEP,FANCCn.410+21024T>C
n.2395A>G
c.1580A>G (p.Asp527Gly)
c.1725A>G (n.1725A>G)
c.899A>G (p.Asp300Gly)
c.1415A>G (p.Asp472Gly)
c.1124A>G (p.Asp375Gly)
c.2319+21024T>C (n.2319+21024T>C)
c.959A>G (p.Asp320Gly)
9g.95101804T>GCA374104644AOPEP,FANCCn.410+21024T>G
n.2395A>C
c.1580A>C (p.Asp527Ala)
c.1725A>C (n.1725A>C)
c.899A>C (p.Asp300Ala)
c.1415A>C (p.Asp472Ala)
c.1124A>C (p.Asp375Ala)
c.2319+21024T>G (n.2319+21024T>G)
c.959A>C (p.Asp320Ala)
9g.95101805C>ACA374104647AOPEP,FANCCn.410+21025C>A
n.2394G>T
c.1579G>T (p.Asp527Tyr)
c.1724G>T (n.1724G>T)
c.898G>T (p.Asp300Tyr)
c.1414G>T (p.Asp472Tyr)
c.1123G>T (p.Asp375Tyr)
c.2319+21025C>A (n.2319+21025C>A)
c.958G>T (p.Asp320Tyr)
 gnomAD v4
9g.95101805C>GCA374104652AOPEP,FANCCn.410+21025C>G
n.2394G>C
c.1579G>C (p.Asp527His)
c.1724G>C (n.1724G>C)
c.898G>C (p.Asp300His)
c.1414G>C (p.Asp472His)
c.1123G>C (p.Asp375His)
c.2319+21025C>G (n.2319+21025C>G)
c.958G>C (p.Asp320His)
9g.95101805C>TCA374104649AOPEP,FANCCn.410+21025C>T
n.2394G>A
c.1579G>A (p.Asp527Asn)
c.1724G>A (n.1724G>A)
c.898G>A (p.Asp300Asn)
c.1414G>A (p.Asp472Asn)
c.1123G>A (p.Asp375Asn)
c.2319+21025C>T (n.2319+21025C>T)
c.958G>A (p.Asp320Asn)
 gnomAD v4
9g.95101806A=CA1865459558AOPEP,FANCCn.410+21026A=
n.2393T=
c.1578T= (p.Leu526=)
c.1723T= (n.1723T=)
c.897T= (p.Leu299=)
c.1413T= (p.Leu471=)
c.1122T= (p.Leu374=)
c.2319+21026A= (n.2319+21026A=)
c.957T= (p.Leu319=)
9g.95101806A>CCA466092094AOPEP,FANCCn.410+21026A>C
n.2393T>G
c.1578T>G (p.Leu526=)
c.1723T>G (n.1723T>G)
c.897T>G (p.Leu299=)
c.1413T>G (p.Leu471=)
c.1122T>G (p.Leu374=)
c.2319+21026A>C (n.2319+21026A>C)
c.957T>G (p.Leu319=)
 ClinVar dbSNP
9g.95101806A>GCA466092093AOPEP,FANCCn.410+21026A>G
n.2393T>C
c.1578T>C (p.Leu526=)
c.1723T>C (n.1723T>C)
c.897T>C (p.Leu299=)
c.1413T>C (p.Leu471=)
c.1122T>C (p.Leu374=)
c.2319+21026A>G (n.2319+21026A>G)
c.957T>C (p.Leu319=)
9g.95101806A>TCA466092092AOPEP,FANCCn.410+21026A>T
n.2393T>A
c.1578T>A (p.Leu526=)
c.1723T>A (n.1723T>A)
c.897T>A (p.Leu299=)
c.1413T>A (p.Leu471=)
c.1122T>A (p.Leu374=)
c.2319+21026A>T (n.2319+21026A>T)
c.957T>A (p.Leu319=)
 ClinVar gnomAD v4
9g.95101807A>CCA374104655AOPEP,FANCCn.410+21027A>C
n.2392T>G
c.1577T>G (p.Leu526Arg)
c.1722T>G (n.1722T>G)
c.896T>G (p.Leu299Arg)
c.1412T>G (p.Leu471Arg)
c.1121T>G (p.Leu374Arg)
c.2319+21027A>C (n.2319+21027A>C)
c.956T>G (p.Leu319Arg)
9g.95101807A>GCA374104657AOPEP,FANCCn.410+21027A>G
n.2392T>C
c.1577T>C (p.Leu526Pro)
c.1722T>C (n.1722T>C)
c.896T>C (p.Leu299Pro)
c.1412T>C (p.Leu471Pro)
c.1121T>C (p.Leu374Pro)
c.2319+21027A>G (n.2319+21027A>G)
c.956T>C (p.Leu319Pro)
 gnomAD v4
9g.95101807A>TCA374104659AOPEP,FANCCn.410+21027A>T
n.2392T>A
c.1577T>A (p.Leu526His)
c.1722T>A (n.1722T>A)
c.896T>A (p.Leu299His)
c.1412T>A (p.Leu471His)
c.1121T>A (p.Leu374His)
c.2319+21027A>T (n.2319+21027A>T)
c.956T>A (p.Leu319His)
9g.95101808G>ACA374104662AOPEP,FANCCn.410+21028G>A
n.2391C>T
c.1576C>T (p.Leu526Phe)
c.1721C>T (n.1721C>T)
c.895C>T (p.Leu299Phe)
c.1411C>T (p.Leu471Phe)
c.1120C>T (p.Leu374Phe)
c.2319+21028G>A (n.2319+21028G>A)
c.955C>T (p.Leu319Phe)
9g.95101808G>CCA374104664AOPEP,FANCCn.410+21028G>C
n.2391C>G
c.1576C>G (p.Leu526Val)
c.1721C>G (n.1721C>G)
c.895C>G (p.Leu299Val)
c.1411C>G (p.Leu471Val)
c.1120C>G (p.Leu374Val)
c.2319+21028G>C (n.2319+21028G>C)
c.955C>G (p.Leu319Val)
9g.95101808G>TCA374104666AOPEP,FANCCn.410+21028G>T
n.2391C>A
c.1576C>A (p.Leu526Ile)
c.1721C>A (n.1721C>A)
c.895C>A (p.Leu299Ile)
c.1411C>A (p.Leu471Ile)
c.1120C>A (p.Leu374Ile)
c.2319+21028G>T (n.2319+21028G>T)
c.955C>A (p.Leu319Ile)
9g.95101809A=CA1865459559AOPEP,FANCCn.410+21029A=
n.2390T=
c.1575T= (p.Phe525=)
c.1720T= (n.1720T=)
c.894T= (p.Phe298=)
c.1410T= (p.Phe470=)
c.1119T= (p.Phe373=)
c.2319+21029A= (n.2319+21029A=)
c.954T= (p.Phe318=)
9g.95101809A>CCA287193AOPEP,FANCCn.410+21029A>C
n.2390T>G
c.1575T>G (p.Phe525Leu)
c.1720T>G (n.1720T>G)
c.894T>G (p.Phe298Leu)
c.1410T>G (p.Phe470Leu)
c.1119T>G (p.Phe373Leu)
c.2319+21029A>C (n.2319+21029A>C)
c.954T>G (p.Phe318Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.95101809A>GCA466092095AOPEP,FANCCn.410+21029A>G
n.2390T>C
c.1575T>C (p.Phe525=)
c.1720T>C (n.1720T>C)
c.894T>C (p.Phe298=)
c.1410T>C (p.Phe470=)
c.1119T>C (p.Phe373=)
c.2319+21029A>G (n.2319+21029A>G)
c.954T>C (p.Phe318=)
 gnomAD v4
9g.95101809A>TCA374104669AOPEP,FANCCn.410+21029A>T
n.2390T>A
c.1575T>A (p.Phe525Leu)
c.1720T>A (n.1720T>A)
c.894T>A (p.Phe298Leu)
c.1410T>A (p.Phe470Leu)
c.1119T>A (p.Phe373Leu)
c.2319+21029A>T (n.2319+21029A>T)
c.954T>A (p.Phe318Leu)
9g.95101810A>CCA374104671AOPEP,FANCCn.410+21030A>C
n.2389T>G
c.1574T>G (p.Phe525Cys)
c.1719T>G (n.1719T>G)
c.893T>G (p.Phe298Cys)
c.1409T>G (p.Phe470Cys)
c.1118T>G (p.Phe373Cys)
c.2319+21030A>C (n.2319+21030A>C)
c.953T>G (p.Phe318Cys)
9g.95101810A>GCA374104674AOPEP,FANCCn.410+21030A>G
n.2389T>C
c.1574T>C (p.Phe525Ser)
c.1719T>C (n.1719T>C)
c.893T>C (p.Phe298Ser)
c.1409T>C (p.Phe470Ser)
c.1118T>C (p.Phe373Ser)
c.2319+21030A>G (n.2319+21030A>G)
c.953T>C (p.Phe318Ser)

Number of alleles fetched