Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.67782848A=CA2144027650ZFYVE26c.4304T= (p.Val1435=)
n.4441T=
c.*2350+251T= (n.*2350+251T=)
c.2795T= (p.Val932=)
c.1979T= (p.Val660=)
c.1886T= (p.Val629=)
14g.67782848A>CCA390170191ZFYVE26c.4304T>G (p.Val1435Gly)
n.4441T>G
c.*2350+251T>G (n.*2350+251T>G)
c.2795T>G (p.Val932Gly)
c.1979T>G (p.Val660Gly)
c.1886T>G (p.Val629Gly)
ClinVar dbSNP
14g.67782848A>GCA390170193ZFYVE26c.4304T>C (p.Val1435Ala)
n.4441T>C
c.*2350+251T>C (n.*2350+251T>C)
c.2795T>C (p.Val932Ala)
c.1979T>C (p.Val660Ala)
c.1886T>C (p.Val629Ala)
14g.67782848A>TCA390170194ZFYVE26c.4304T>A (p.Val1435Glu)
n.4441T>A
c.*2350+251T>A (n.*2350+251T>A)
c.2795T>A (p.Val932Glu)
c.1979T>A (p.Val660Glu)
c.1886T>A (p.Val629Glu)
ClinVar
14g.67782849C>ACA390170197ZFYVE26c.4303G>T (p.Val1435Leu)
n.4440G>T
c.*2350+250G>T (n.*2350+250G>T)
c.2794G>T (p.Val932Leu)
c.1978G>T (p.Val660Leu)
c.1885G>T (p.Val629Leu)
14g.67782849C=CA2144027651ZFYVE26c.4303G= (p.Val1435=)
n.4440G=
c.*2350+250G= (n.*2350+250G=)
c.2794G= (p.Val932=)
c.1978G= (p.Val660=)
c.1885G= (p.Val629=)
14g.67782849C>GCA390170199ZFYVE26c.4303G>C (p.Val1435Leu)
n.4440G>C
c.*2350+250G>C (n.*2350+250G>C)
c.2794G>C (p.Val932Leu)
c.1978G>C (p.Val660Leu)
c.1885G>C (p.Val629Leu)
14g.67782849C>TCA262848523ZFYVE26c.4303G>A (p.Val1435Met)
n.4440G>A
c.*2350+250G>A (n.*2350+250G>A)
c.2794G>A (p.Val932Met)
c.1978G>A (p.Val660Met)
c.1885G>A (p.Val629Met)
dbSNP
14g.67782850T>ACA390170202ZFYVE26c.4302A>T (p.Glu1434Asp)
n.4439A>T
c.*2350+249A>T (n.*2350+249A>T)
c.2793A>T (p.Glu931Asp)
c.1977A>T (p.Glu659Asp)
c.1884A>T (p.Glu628Asp)
ClinVar dbSNP
14g.67782850T>CCA7239801ZFYVE26c.4302A>G (p.Glu1434=)
n.4439A>G
c.*2350+249A>G (n.*2350+249A>G)
c.2793A>G (p.Glu931=)
c.1977A>G (p.Glu659=)
c.1884A>G (p.Glu628=)
dbSNP ExAC gnomAD v4
14g.67782850T>GCA390170204ZFYVE26c.4302A>C (p.Glu1434Asp)
n.4439A>C
c.*2350+249A>C (n.*2350+249A>C)
c.2793A>C (p.Glu931Asp)
c.1977A>C (p.Glu659Asp)
c.1884A>C (p.Glu628Asp)
14g.67782850T=CA2144027652ZFYVE26c.4302A= (p.Glu1434=)
n.4439A=
c.*2350+249A= (n.*2350+249A=)
c.2793A= (p.Glu931=)
c.1977A= (p.Glu659=)
c.1884A= (p.Glu628=)
14g.67782851T>ACA390170206ZFYVE26c.4301A>T (p.Glu1434Val)
n.4438A>T
c.*2350+248A>T (n.*2350+248A>T)
c.2792A>T (p.Glu931Val)
c.1976A>T (p.Glu659Val)
c.1883A>T (p.Glu628Val)
14g.67782851T>CCA390170208ZFYVE26c.4301A>G (p.Glu1434Gly)
n.4438A>G
c.*2350+248A>G (n.*2350+248A>G)
c.2792A>G (p.Glu931Gly)
c.1976A>G (p.Glu659Gly)
c.1883A>G (p.Glu628Gly)
14g.67782851T>GCA7239802ZFYVE26c.4301A>C (p.Glu1434Ala)
n.4438A>C
c.*2350+248A>C (n.*2350+248A>C)
c.2792A>C (p.Glu931Ala)
c.1976A>C (p.Glu659Ala)
c.1883A>C (p.Glu628Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.67782851T=CA2144027653ZFYVE26c.4301A= (p.Glu1434=)
n.4438A=
c.*2350+248A= (n.*2350+248A=)
c.2792A= (p.Glu931=)
c.1976A= (p.Glu659=)
c.1883A= (p.Glu628=)
14g.67782852C>ACA390170211ZFYVE26c.4300G>T (p.Glu1434Ter)
n.4437G>T
c.*2350+247G>T (n.*2350+247G>T)
c.2791G>T (p.Glu931Ter)
c.1975G>T (p.Glu659Ter)
c.1882G>T (p.Glu628Ter)
14g.67782852C>GCA390170213ZFYVE26c.4300G>C (p.Glu1434Gln)
n.4437G>C
c.*2350+247G>C (n.*2350+247G>C)
c.2791G>C (p.Glu931Gln)
c.1975G>C (p.Glu659Gln)
c.1882G>C (p.Glu628Gln)
14g.67782852C>TCA390170215ZFYVE26c.4300G>A (p.Glu1434Lys)
n.4437G>A
c.*2350+247G>A (n.*2350+247G>A)
c.2791G>A (p.Glu931Lys)
c.1975G>A (p.Glu659Lys)
c.1882G>A (p.Glu628Lys)
14g.67782853A>CCA486970555ZFYVE26c.4299T>G (p.Thr1433=)
n.4436T>G
c.*2350+246T>G (n.*2350+246T>G)
c.2790T>G (p.Thr930=)
c.1974T>G (p.Thr658=)
c.1881T>G (p.Thr627=)
14g.67782853A>GCA486970557ZFYVE26c.4299T>C (p.Thr1433=)
n.4436T>C
c.*2350+246T>C (n.*2350+246T>C)
c.2790T>C (p.Thr930=)
c.1974T>C (p.Thr658=)
c.1881T>C (p.Thr627=)
14g.67782853A>TCA486970559ZFYVE26c.4299T>A (p.Thr1433=)
n.4436T>A
c.*2350+246T>A (n.*2350+246T>A)
c.2790T>A (p.Thr930=)
c.1974T>A (p.Thr658=)
c.1881T>A (p.Thr627=)
14g.67782854G>ACA390170216ZFYVE26c.4298C>T (p.Thr1433Ile)
n.4435C>T
c.*2350+245C>T (n.*2350+245C>T)
c.2789C>T (p.Thr930Ile)
c.1973C>T (p.Thr658Ile)
c.1880C>T (p.Thr627Ile)
14g.67782854G>CCA390170218ZFYVE26c.4298C>G (p.Thr1433Ser)
n.4435C>G
c.*2350+245C>G (n.*2350+245C>G)
c.2789C>G (p.Thr930Ser)
c.1973C>G (p.Thr658Ser)
c.1880C>G (p.Thr627Ser)
14g.67782854G>TCA390170220ZFYVE26c.4298C>A (p.Thr1433Asn)
n.4435C>A
c.*2350+245C>A (n.*2350+245C>A)
c.2789C>A (p.Thr930Asn)
c.1973C>A (p.Thr658Asn)
c.1880C>A (p.Thr627Asn)
14g.67782855T>ACA390170224ZFYVE26c.4297A>T (p.Thr1433Ser)
n.4434A>T
c.*2350+244A>T (n.*2350+244A>T)
c.2788A>T (p.Thr930Ser)
c.1972A>T (p.Thr658Ser)
c.1879A>T (p.Thr627Ser)
14g.67782855T>CCA7239803ZFYVE26c.4297A>G (p.Thr1433Ala)
n.4434A>G
c.*2350+244A>G (n.*2350+244A>G)
c.2788A>G (p.Thr930Ala)
c.1972A>G (p.Thr658Ala)
c.1879A>G (p.Thr627Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.67782855T>GCA390170222ZFYVE26c.4297A>C (p.Thr1433Pro)
n.4434A>C
c.*2350+244A>C (n.*2350+244A>C)
c.2788A>C (p.Thr930Pro)
c.1972A>C (p.Thr658Pro)
c.1879A>C (p.Thr627Pro)
14g.67782855T=CA2144027654ZFYVE26c.4297A= (p.Thr1433=)
n.4434A=
c.*2350+244A= (n.*2350+244A=)
c.2788A= (p.Thr930=)
c.1972A= (p.Thr658=)
c.1879A= (p.Thr627=)
14g.67782856G>ACA486970563ZFYVE26c.4296C>T (p.Leu1432=)
n.4433C>T
c.*2350+243C>T (n.*2350+243C>T)
c.2787C>T (p.Leu929=)
c.1971C>T (p.Leu657=)
c.1878C>T (p.Leu626=)
gnomAD v4
14g.67782856G>CCA486970564ZFYVE26c.4296C>G (p.Leu1432=)
n.4433C>G
c.*2350+243C>G (n.*2350+243C>G)
c.2787C>G (p.Leu929=)
c.1971C>G (p.Leu657=)
c.1878C>G (p.Leu626=)
14g.67782856G>TCA486970565ZFYVE26c.4296C>A (p.Leu1432=)
n.4433C>A
c.*2350+243C>A (n.*2350+243C>A)
c.2787C>A (p.Leu929=)
c.1971C>A (p.Leu657=)
c.1878C>A (p.Leu626=)
14g.67782857A>CCA390170226ZFYVE26c.4295T>G (p.Leu1432Arg)
n.4432T>G
c.*2350+242T>G (n.*2350+242T>G)
c.2786T>G (p.Leu929Arg)
c.1970T>G (p.Leu657Arg)
c.1877T>G (p.Leu626Arg)
14g.67782857A>GCA390170228ZFYVE26c.4295T>C (p.Leu1432Pro)
n.4432T>C
c.*2350+242T>C (n.*2350+242T>C)
c.2786T>C (p.Leu929Pro)
c.1970T>C (p.Leu657Pro)
c.1877T>C (p.Leu626Pro)
14g.67782857A>TCA390170229ZFYVE26c.4295T>A (p.Leu1432His)
n.4432T>A
c.*2350+242T>A (n.*2350+242T>A)
c.2786T>A (p.Leu929His)
c.1970T>A (p.Leu657His)
c.1877T>A (p.Leu626His)
14g.67782858G>ACA390170231ZFYVE26c.4294C>T (p.Leu1432Phe)
n.4431C>T
c.*2350+241C>T (n.*2350+241C>T)
c.2785C>T (p.Leu929Phe)
c.1969C>T (p.Leu657Phe)
c.1876C>T (p.Leu626Phe)
dbSNP gnomAD v4
14g.67782858G>CCA390170233ZFYVE26c.4294C>G (p.Leu1432Val)
n.4431C>G
c.*2350+241C>G (n.*2350+241C>G)
c.2785C>G (p.Leu929Val)
c.1969C>G (p.Leu657Val)
c.1876C>G (p.Leu626Val)
14g.67782858G=CA2144027655ZFYVE26c.4294C= (p.Leu1432=)
n.4431C=
c.*2350+241C= (n.*2350+241C=)
c.2785C= (p.Leu929=)
c.1969C= (p.Leu657=)
c.1876C= (p.Leu626=)
14g.67782858G>TCA390170235ZFYVE26c.4294C>A (p.Leu1432Ile)
n.4431C>A
c.*2350+241C>A (n.*2350+241C>A)
c.2785C>A (p.Leu929Ile)
c.1969C>A (p.Leu657Ile)
c.1876C>A (p.Leu626Ile)
14g.67782859C>ACA390170237ZFYVE26c.4293G>T (p.Gln1431His)
n.4430G>T
c.*2350+240G>T (n.*2350+240G>T)
c.2784G>T (p.Gln928His)
c.1968G>T (p.Gln656His)
c.1875G>T (p.Gln625His)
gnomAD v4
14g.67782859C=CA2144027656ZFYVE26c.4293G= (p.Gln1431=)
n.4430G=
c.*2350+240G= (n.*2350+240G=)
c.2784G= (p.Gln928=)
c.1968G= (p.Gln656=)
c.1875G= (p.Gln625=)
14g.67782859C>GCA7239804ZFYVE26c.4293G>C (p.Gln1431His)
n.4430G>C
c.*2350+240G>C (n.*2350+240G>C)
c.2784G>C (p.Gln928His)
c.1968G>C (p.Gln656His)
c.1875G>C (p.Gln625His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.67782859C>TCA486970570ZFYVE26c.4293G>A (p.Gln1431=)
n.4430G>A
c.*2350+240G>A (n.*2350+240G>A)
c.2784G>A (p.Gln928=)
c.1968G>A (p.Gln656=)
c.1875G>A (p.Gln625=)
COSMIC
14g.67782860T>ACA390170240ZFYVE26c.4292A>T (p.Gln1431Leu)
n.4429A>T
c.*2350+239A>T (n.*2350+239A>T)
c.2783A>T (p.Gln928Leu)
c.1967A>T (p.Gln656Leu)
c.1874A>T (p.Gln625Leu)
14g.67782860T>CCA390170241ZFYVE26c.4292A>G (p.Gln1431Arg)
n.4429A>G
c.*2350+239A>G (n.*2350+239A>G)
c.2783A>G (p.Gln928Arg)
c.1967A>G (p.Gln656Arg)
c.1874A>G (p.Gln625Arg)
14g.67782860T>GCA390170243ZFYVE26c.4292A>C (p.Gln1431Pro)
n.4429A>C
c.*2350+239A>C (n.*2350+239A>C)
c.2783A>C (p.Gln928Pro)
c.1967A>C (p.Gln656Pro)
c.1874A>C (p.Gln625Pro)
14g.67782861G>ACA390170249ZFYVE26c.4291C>T (p.Gln1431Ter)
n.4428C>T
c.*2350+238C>T (n.*2350+238C>T)
c.2782C>T (p.Gln928Ter)
c.1966C>T (p.Gln656Ter)
c.1873C>T (p.Gln625Ter)
ClinVar dbSNP
14g.67782861G>CCA390170247ZFYVE26c.4291C>G (p.Gln1431Glu)
n.4428C>G
c.*2350+238C>G (n.*2350+238C>G)
c.2782C>G (p.Gln928Glu)
c.1966C>G (p.Gln656Glu)
c.1873C>G (p.Gln625Glu)
14g.67782861G>TCA390170245ZFYVE26c.4291C>A (p.Gln1431Lys)
n.4428C>A
c.*2350+238C>A (n.*2350+238C>A)
c.2782C>A (p.Gln928Lys)
c.1966C>A (p.Gln656Lys)
c.1873C>A (p.Gln625Lys)
14g.67782862A>CCA486970576ZFYVE26c.4290T>G (p.Leu1430=)
n.4427T>G
c.*2350+237T>G (n.*2350+237T>G)
c.2781T>G (p.Leu927=)
c.1965T>G (p.Leu655=)
c.1872T>G (p.Leu624=)

Number of alleles fetched