Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.92718915G>ACA5126496BICD2c.1730C>T (p.Ala577Val)
c.1811C>T (p.Ala604Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
9g.92718915G>CCA374036167BICD2c.1730C>G (p.Ala577Gly)
c.1811C>G (p.Ala604Gly)
9g.92718915G=CA1864361203BICD2c.1730C= (p.Ala577=)
c.1811C= (p.Ala604=)
9g.92718915G>TCA374036168BICD2c.1730C>A (p.Ala577Glu)
c.1811C>A (p.Ala604Glu)
gnomAD v4
9g.92718916C>ACA374036169BICD2c.1729G>T (p.Ala577Ser)
c.1810G>T (p.Ala604Ser)
gnomAD v4
9g.92718916C>GCA374036170BICD2c.1729G>C (p.Ala577Pro)
c.1810G>C (p.Ala604Pro)
9g.92718916C>TCA374036171BICD2c.1729G>A (p.Ala577Thr)
c.1810G>A (p.Ala604Thr)
gnomAD v4
9g.92718917C>ACA374036173BICD2c.1728G>T (p.Glu576Asp)
c.1809G>T (p.Glu603Asp)
9g.92718917C>GCA374036175BICD2c.1728G>C (p.Glu576Asp)
c.1809G>C (p.Glu603Asp)
9g.92718917C>TCA466343042BICD2c.1728G>A (p.Glu576=)
c.1809G>A (p.Glu603=)
gnomAD v4
9g.92718918T>ACA374036181BICD2c.1727A>T (p.Glu576Val)
c.1808A>T (p.Glu603Val)
9g.92718918T>CCA196340249BICD2c.1727A>G (p.Glu576Gly)
c.1808A>G (p.Glu603Gly)
dbSNP gnomAD v4
9g.92718918T>GCA374036176BICD2c.1727A>C (p.Glu576Ala)
c.1808A>C (p.Glu603Ala)
9g.92718918T=CA1864361206BICD2c.1727A= (p.Glu576=)
c.1808A= (p.Glu603=)
9g.92718918_92718936delinsTCGGGGCTGGTGCGGCCCCCA1864361208BICD2c.1709_1727delinsGGGGCCGCACCAGCCCCGA (p.Gly570=)
c.1790_1808delinsGGGGCCGCACCAGCCCCGA (p.Gly597=)
9g.92718919C>ACA374036184BICD2c.1726G>T (p.Glu576Ter)
c.1807G>T (p.Glu603Ter)
9g.92718919C>GCA374036186BICD2c.1726G>C (p.Glu576Gln)
c.1807G>C (p.Glu603Gln)
9g.92718919C>TCA374036189BICD2c.1726G>A (p.Glu576Lys)
c.1807G>A (p.Glu603Lys)
gnomAD v4
9g.92718923_92718940delCA589579138BICD2c.1709_1726del (p.Gly570_Pro575del)
c.1790_1807del (p.Gly597_Pro602del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.92718920G>ACA5126497BICD2c.1725C>T (p.Pro575=)
c.1806C>T (p.Pro602=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.92718920G>CCA5126498BICD2c.1725C>G (p.Pro575=)
c.1806C>G (p.Pro602=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.92718920G=CA1864361221BICD2c.1725C= (p.Pro575=)
c.1806C= (p.Pro602=)
9g.92718920G>TCA466343044BICD2c.1725C>A (p.Pro575=)
c.1806C>A (p.Pro602=)
gnomAD v4
9g.92718921G>ACA374036195BICD2c.1724C>T (p.Pro575Leu)
c.1805C>T (p.Pro602Leu)
9g.92718921G>CCA374036198BICD2c.1724C>G (p.Pro575Arg)
c.1805C>G (p.Pro602Arg)
9g.92718921G=CA1864361229BICD2c.1724C= (p.Pro575=)
c.1805C= (p.Pro602=)
9g.92718921G>TCA5126499BICD2c.1724C>A (p.Pro575His)
c.1805C>A (p.Pro602His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
9g.92718922G>ACA5126500BICD2c.1723C>T (p.Pro575Ser)
c.1804C>T (p.Pro602Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.92718922G>CCA374036200BICD2c.1723C>G (p.Pro575Ala)
c.1804C>G (p.Pro602Ala)
9g.92718922G=CA1864361233BICD2c.1723C= (p.Pro575=)
c.1804C= (p.Pro602=)
9g.92718922G>TCA374036201BICD2c.1723C>A (p.Pro575Thr)
c.1804C>A (p.Pro602Thr)
gnomAD v4
9g.92718923G>ACA196340312BICD2c.1722C>T (p.Ser574=)
c.1803C>T (p.Ser601=)
dbSNP gnomAD v2
9g.92718923G>CCA374036205BICD2c.1722C>G (p.Ser574Arg)
c.1803C>G (p.Ser601Arg)
9g.92718923G=CA1864361237BICD2c.1722C= (p.Ser574=)
c.1803C= (p.Ser601=)
9g.92718923G>TCA374036202BICD2c.1722C>A (p.Ser574Arg)
c.1803C>A (p.Ser601Arg)
9g.92718923_92718941delinsGCTGGTGCGGCCCCCGGGACA1864361239BICD2c.1704_1722delinsTCCCGGGGGCCGCACCAGC (p.Ser568=)
c.1785_1803delinsTCCCGGGGGCCGCACCAGC (p.Ser595=)
9g.92718924C>ACA374036207BICD2c.1721G>T (p.Ser574Ile)
c.1802G>T (p.Ser601Ile)
9g.92718924C=CA1864361248BICD2c.1721G= (p.Ser574=)
c.1802G= (p.Ser601=)
9g.92718924C>GCA374036209BICD2c.1721G>C (p.Ser574Thr)
c.1802G>C (p.Ser601Thr)
9g.92718924C>TCA196340316BICD2c.1721G>A (p.Ser574Asn)
c.1802G>A (p.Ser601Asn)
dbSNP gnomAD v2 gnomAD v4
9g.92718935_92718952dupCA196340315BICD2c.1704_1721dup (p.Ser574_Pro575insProGlyGlyArgThrSer)
c.1785_1802dup (p.Ser601_Pro602insProGlyGlyArgThrSer)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.92718935_92718952delCA868524750BICD2c.1704_1721del (p.Pro569_Ser574del)
c.1785_1802del (p.Pro596_Ser601del)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.92718925T>ACA374036212BICD2c.1720A>T (p.Ser574Cys)
c.1801A>T (p.Ser601Cys)
dbSNP gnomAD v3 gnomAD v4
9g.92718925T>CCA374036214BICD2c.1720A>G (p.Ser574Gly)
c.1801A>G (p.Ser601Gly)
9g.92718925T>GCA374036215BICD2c.1720A>C (p.Ser574Arg)
c.1801A>C (p.Ser601Arg)
9g.92718926G>ACA466343054BICD2c.1719C>T (p.Thr573=)
c.1800C>T (p.Thr600=)
dbSNP gnomAD v4
9g.92718926G>CCA466343056BICD2c.1719C>G (p.Thr573=)
c.1800C>G (p.Thr600=)
9g.92718926G=CA1864361255BICD2c.1719C= (p.Thr573=)
c.1800C= (p.Thr600=)
9g.92718926G>TCA466343058BICD2c.1719C>A (p.Thr573=)
c.1800C>A (p.Thr600=)
ClinVar dbSNP gnomAD v4
9g.92718927G>ACA374036221BICD2c.1718C>T (p.Thr573Ile)
c.1799C>T (p.Thr600Ile)
gnomAD v4

Number of alleles fetched