Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.39357308G>ACA364350087KIF6c.2149C>T (p.His717Tyr)
c.502C>T (p.His168Tyr)
c.1824C>T
c.2098C>T (p.His700Tyr)
c.1981C>T (p.His661Tyr)
c.1522C>T (p.His508Tyr)
c.1840C>T (p.His614Tyr)
c.1504C>T (p.His502Tyr)
n.75+5360G>A
6g.39357308G>CCA364350089KIF6c.2149C>G (p.His717Asp)
c.502C>G (p.His168Asp)
c.1824C>G
c.2098C>G (p.His700Asp)
c.1981C>G (p.His661Asp)
c.1522C>G (p.His508Asp)
c.1840C>G (p.His614Asp)
c.1504C>G (p.His502Asp)
n.75+5360G>C
6g.39357308G>TCA364350091KIF6c.2149C>A (p.His717Asn)
c.502C>A (p.His168Asn)
c.1824C>A
c.2098C>A (p.His700Asn)
c.1981C>A (p.His661Asn)
c.1522C>A (p.His508Asn)
c.1840C>A (p.His614Asn)
c.1504C>A (p.His502Asn)
n.75+5360G>T
6g.39357309C>ACA3793801KIF6c.2148G>T (p.Gln716His)
c.501G>T (p.Gln167His)
c.1823G>T
c.2097G>T (p.Gln699His)
c.1980G>T (p.Gln660His)
c.1521G>T (p.Gln507His)
c.1839G>T (p.Gln613His)
c.1503G>T (p.Gln501His)
n.75+5361C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.39357309C=CA1622646808KIF6c.2148G= (p.Gln716=)
c.501G= (p.Gln167=)
c.1823G=
c.2097G= (p.Gln699=)
c.1980G= (p.Gln660=)
c.1521G= (p.Gln507=)
c.1839G= (p.Gln613=)
c.1503G= (p.Gln501=)
n.75+5361C=
6g.39357309C>GCA3793802KIF6c.2148G>C (p.Gln716His)
c.501G>C (p.Gln167His)
c.1823G>C
c.2097G>C (p.Gln699His)
c.1980G>C (p.Gln660His)
c.1521G>C (p.Gln507His)
c.1839G>C (p.Gln613His)
c.1503G>C (p.Gln501His)
n.75+5361C>G
dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357309C>TCA450098187KIF6c.2148G>A (p.Gln716=)
c.501G>A (p.Gln167=)
c.1823G>A
c.2097G>A (p.Gln699=)
c.1980G>A (p.Gln660=)
c.1521G>A (p.Gln507=)
c.1839G>A (p.Gln613=)
c.1503G>A (p.Gln501=)
n.75+5361C>T
gnomAD v4
6g.39357310T>ACA364350093KIF6c.2147A>T (p.Gln716Leu)
c.500A>T (p.Gln167Leu)
c.1822A>T
c.2096A>T (p.Gln699Leu)
c.1979A>T (p.Gln660Leu)
c.1520A>T (p.Gln507Leu)
c.1838A>T (p.Gln613Leu)
c.1502A>T (p.Gln501Leu)
n.75+5362T>A
6g.39357310T>CCA364350095KIF6c.2147A>G (p.Gln716Arg)
c.500A>G (p.Gln167Arg)
c.1822A>G
c.2096A>G (p.Gln699Arg)
c.1979A>G (p.Gln660Arg)
c.1520A>G (p.Gln507Arg)
c.1838A>G (p.Gln613Arg)
c.1502A>G (p.Gln501Arg)
n.75+5362T>C
6g.39357310T>GCA364350096KIF6c.2147A>C (p.Gln716Pro)
c.500A>C (p.Gln167Pro)
c.1822A>C
c.2096A>C (p.Gln699Pro)
c.1979A>C (p.Gln660Pro)
c.1520A>C (p.Gln507Pro)
c.1838A>C (p.Gln613Pro)
c.1502A>C (p.Gln501Pro)
n.75+5362T>G
6g.39357311G>ACA364350098KIF6c.2146C>T (p.Gln716Ter)
c.499C>T (p.Gln167Ter)
c.1821C>T
c.2095C>T (p.Gln699Ter)
c.1978C>T (p.Gln660Ter)
c.1519C>T (p.Gln507Ter)
c.1837C>T (p.Gln613Ter)
c.1501C>T (p.Gln501Ter)
n.75+5363G>A
6g.39357311G>CCA364350101KIF6c.2146C>G (p.Gln716Glu)
c.499C>G (p.Gln167Glu)
c.1821C>G
c.2095C>G (p.Gln699Glu)
c.1978C>G (p.Gln660Glu)
c.1519C>G (p.Gln507Glu)
c.1837C>G (p.Gln613Glu)
c.1501C>G (p.Gln501Glu)
n.75+5363G>C
6g.39357311G>TCA364350100KIF6c.2146C>A (p.Gln716Lys)
c.499C>A (p.Gln167Lys)
c.1821C>A
c.2095C>A (p.Gln699Lys)
c.1978C>A (p.Gln660Lys)
c.1519C>A (p.Gln507Lys)
c.1837C>A (p.Gln613Lys)
c.1501C>A (p.Gln501Lys)
n.75+5363G>T
COSMIC COSMIC COSMIC COSMIC
6g.39357312G>ACA450098188KIF6c.2145C>T (p.Ser715=)
c.498C>T (p.Ser166=)
c.1820C>T
c.2094C>T (p.Ser698=)
c.1977C>T (p.Ser659=)
c.1518C>T (p.Ser506=)
c.1836C>T (p.Ser612=)
c.1500C>T (p.Ser500=)
n.75+5364G>A
6g.39357312G>CCA450098189KIF6c.2145C>G (p.Ser715=)
c.498C>G (p.Ser166=)
c.1820C>G
c.2094C>G (p.Ser698=)
c.1977C>G (p.Ser659=)
c.1518C>G (p.Ser506=)
c.1836C>G (p.Ser612=)
c.1500C>G (p.Ser500=)
n.75+5364G>C
6g.39357312G>TCA450098190KIF6c.2145C>A (p.Ser715=)
c.498C>A (p.Ser166=)
c.1820C>A
c.2094C>A (p.Ser698=)
c.1977C>A (p.Ser659=)
c.1518C>A (p.Ser506=)
c.1836C>A (p.Ser612=)
c.1500C>A (p.Ser500=)
n.75+5364G>T
6g.39357313G>ACA364350102KIF6c.2144C>T (p.Ser715Phe)
c.497C>T (p.Ser166Phe)
c.1819C>T
c.2093C>T (p.Ser698Phe)
c.1976C>T (p.Ser659Phe)
c.1517C>T (p.Ser506Phe)
c.1835C>T (p.Ser612Phe)
c.1499C>T (p.Ser500Phe)
n.75+5365G>A
6g.39357313G>CCA364350103KIF6c.2144C>G (p.Ser715Cys)
c.497C>G (p.Ser166Cys)
c.1819C>G
c.2093C>G (p.Ser698Cys)
c.1976C>G (p.Ser659Cys)
c.1517C>G (p.Ser506Cys)
c.1835C>G (p.Ser612Cys)
c.1499C>G (p.Ser500Cys)
n.75+5365G>C
6g.39357313G>TCA364350104KIF6c.2144C>A (p.Ser715Tyr)
c.497C>A (p.Ser166Tyr)
c.1819C>A
c.2093C>A (p.Ser698Tyr)
c.1976C>A (p.Ser659Tyr)
c.1517C>A (p.Ser506Tyr)
c.1835C>A (p.Ser612Tyr)
c.1499C>A (p.Ser500Tyr)
n.75+5365G>T
6g.39357314A>CCA364350106KIF6c.2143T>G (p.Ser715Ala)
c.496T>G (p.Ser166Ala)
c.1818T>G
c.2092T>G (p.Ser698Ala)
c.1975T>G (p.Ser659Ala)
c.1516T>G (p.Ser506Ala)
c.1834T>G (p.Ser612Ala)
c.1498T>G (p.Ser500Ala)
n.75+5366A>C
6g.39357314A>GCA364350107KIF6c.2143T>C (p.Ser715Pro)
c.496T>C (p.Ser166Pro)
c.1818T>C
c.2092T>C (p.Ser698Pro)
c.1975T>C (p.Ser659Pro)
c.1516T>C (p.Ser506Pro)
c.1834T>C (p.Ser612Pro)
c.1498T>C (p.Ser500Pro)
n.75+5366A>G
gnomAD v4
6g.39357314A>TCA364350109KIF6c.2143T>A (p.Ser715Thr)
c.496T>A (p.Ser166Thr)
c.1818T>A
c.2092T>A (p.Ser698Thr)
c.1975T>A (p.Ser659Thr)
c.1516T>A (p.Ser506Thr)
c.1834T>A (p.Ser612Thr)
c.1498T>A (p.Ser500Thr)
n.75+5366A>T
6g.39357315G>ACA137717071KIF6c.2142C>T (p.Asp714=)
c.495C>T (p.Asp165=)
c.1817C>T
c.2091C>T (p.Asp697=)
c.1974C>T (p.Asp658=)
c.1515C>T (p.Asp505=)
c.1833C>T (p.Asp611=)
c.1497C>T (p.Asp499=)
n.75+5367G>A
dbSNP
6g.39357315G>CCA364350113KIF6c.2142C>G (p.Asp714Glu)
c.495C>G (p.Asp165Glu)
c.1817C>G
c.2091C>G (p.Asp697Glu)
c.1974C>G (p.Asp658Glu)
c.1515C>G (p.Asp505Glu)
c.1833C>G (p.Asp611Glu)
c.1497C>G (p.Asp499Glu)
n.75+5367G>C
6g.39357315G=CA1622646811KIF6c.2142C= (p.Asp714=)
c.495C= (p.Asp165=)
c.1817C=
c.2091C= (p.Asp697=)
c.1974C= (p.Asp658=)
c.1515C= (p.Asp505=)
c.1833C= (p.Asp611=)
c.1497C= (p.Asp499=)
n.75+5367G=
6g.39357315G>TCA364350111KIF6c.2142C>A (p.Asp714Glu)
c.495C>A (p.Asp165Glu)
c.1817C>A
c.2091C>A (p.Asp697Glu)
c.1974C>A (p.Asp658Glu)
c.1515C>A (p.Asp505Glu)
c.1833C>A (p.Asp611Glu)
c.1497C>A (p.Asp499Glu)
n.75+5367G>T
6g.39357316T>ACA364350115KIF6c.2141A>T (p.Asp714Val)
c.494A>T (p.Asp165Val)
c.1816A>T
c.2090A>T (p.Asp697Val)
c.1973A>T (p.Asp658Val)
c.1514A>T (p.Asp505Val)
c.1832A>T (p.Asp611Val)
c.1496A>T (p.Asp499Val)
n.75+5368T>A
COSMIC COSMIC
6g.39357316T>CCA364350117KIF6c.2141A>G (p.Asp714Gly)
c.494A>G (p.Asp165Gly)
c.1816A>G
c.2090A>G (p.Asp697Gly)
c.1973A>G (p.Asp658Gly)
c.1514A>G (p.Asp505Gly)
c.1832A>G (p.Asp611Gly)
c.1496A>G (p.Asp499Gly)
n.75+5368T>C
6g.39357316T>GCA364350118KIF6c.2141A>C (p.Asp714Ala)
c.494A>C (p.Asp165Ala)
c.1816A>C
c.2090A>C (p.Asp697Ala)
c.1973A>C (p.Asp658Ala)
c.1514A>C (p.Asp505Ala)
c.1832A>C (p.Asp611Ala)
c.1496A>C (p.Asp499Ala)
n.75+5368T>G
gnomAD v4
6g.39357317C>ACA364350119KIF6c.2140G>T (p.Asp714Tyr)
c.493G>T (p.Asp165Tyr)
c.1815G>T
c.2089G>T (p.Asp697Tyr)
c.1972G>T (p.Asp658Tyr)
c.1513G>T (p.Asp505Tyr)
c.1831G>T (p.Asp611Tyr)
c.1495G>T (p.Asp499Tyr)
n.75+5369C>A
6g.39357317C>GCA364350120KIF6c.2140G>C (p.Asp714His)
c.493G>C (p.Asp165His)
c.1815G>C
c.2089G>C (p.Asp697His)
c.1972G>C (p.Asp658His)
c.1513G>C (p.Asp505His)
c.1831G>C (p.Asp611His)
c.1495G>C (p.Asp499His)
n.75+5369C>G
6g.39357317C>TCA364350121KIF6c.2140G>A (p.Asp714Asn)
c.493G>A (p.Asp165Asn)
c.1815G>A
c.2089G>A (p.Asp697Asn)
c.1972G>A (p.Asp658Asn)
c.1513G>A (p.Asp505Asn)
c.1831G>A (p.Asp611Asn)
c.1495G>A (p.Asp499Asn)
n.75+5369C>T
6g.39357318A>CCA450098193KIF6c.2139T>G (p.Ser713=)
c.492T>G (p.Ser164=)
c.1814T>G
c.2088T>G (p.Ser696=)
c.1971T>G (p.Ser657=)
c.1512T>G (p.Ser504=)
c.1830T>G (p.Ser610=)
c.1494T>G (p.Ser498=)
n.75+5370A>C
6g.39357318A>GCA450098192KIF6c.2139T>C (p.Ser713=)
c.492T>C (p.Ser164=)
c.1814T>C
c.2088T>C (p.Ser696=)
c.1971T>C (p.Ser657=)
c.1512T>C (p.Ser504=)
c.1830T>C (p.Ser610=)
c.1494T>C (p.Ser498=)
n.75+5370A>G
6g.39357318A>TCA450098191KIF6c.2139T>A (p.Ser713=)
c.492T>A (p.Ser164=)
c.1814T>A
c.2088T>A (p.Ser696=)
c.1971T>A (p.Ser657=)
c.1512T>A (p.Ser504=)
c.1830T>A (p.Ser610=)
c.1494T>A (p.Ser498=)
n.75+5370A>T
6g.39357319G>ACA364350122KIF6c.2138C>T (p.Ser713Phe)
c.491C>T (p.Ser164Phe)
c.1813C>T
c.2087C>T (p.Ser696Phe)
c.1970C>T (p.Ser657Phe)
c.1511C>T (p.Ser504Phe)
c.1829C>T (p.Ser610Phe)
c.1493C>T (p.Ser498Phe)
n.75+5371G>A
6g.39357319G>CCA3793803KIF6c.2138C>G (p.Ser713Cys)
c.491C>G (p.Ser164Cys)
c.1813C>G
c.2087C>G (p.Ser696Cys)
c.1970C>G (p.Ser657Cys)
c.1511C>G (p.Ser504Cys)
c.1829C>G (p.Ser610Cys)
c.1493C>G (p.Ser498Cys)
n.75+5371G>C
dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357319G=CA1622646813KIF6c.2138C= (p.Ser713=)
c.491C= (p.Ser164=)
c.1813C=
c.2087C= (p.Ser696=)
c.1970C= (p.Ser657=)
c.1511C= (p.Ser504=)
c.1829C= (p.Ser610=)
c.1493C= (p.Ser498=)
n.75+5371G=
6g.39357319G>TCA364350123KIF6c.2138C>A (p.Ser713Tyr)
c.491C>A (p.Ser164Tyr)
c.1813C>A
c.2087C>A (p.Ser696Tyr)
c.1970C>A (p.Ser657Tyr)
c.1511C>A (p.Ser504Tyr)
c.1829C>A (p.Ser610Tyr)
c.1493C>A (p.Ser498Tyr)
n.75+5371G>T
6g.39357320A>CCA364350125KIF6c.2137T>G (p.Ser713Ala)
c.490T>G (p.Ser164Ala)
c.1812T>G
c.2086T>G (p.Ser696Ala)
c.1969T>G (p.Ser657Ala)
c.1510T>G (p.Ser504Ala)
c.1828T>G (p.Ser610Ala)
c.1492T>G (p.Ser498Ala)
n.75+5372A>C
6g.39357320A>GCA364350126KIF6c.2137T>C (p.Ser713Pro)
c.490T>C (p.Ser164Pro)
c.1812T>C
c.2086T>C (p.Ser696Pro)
c.1969T>C (p.Ser657Pro)
c.1510T>C (p.Ser504Pro)
c.1828T>C (p.Ser610Pro)
c.1492T>C (p.Ser498Pro)
n.75+5372A>G
6g.39357320A>TCA364350128KIF6c.2137T>A (p.Ser713Thr)
c.490T>A (p.Ser164Thr)
c.1812T>A
c.2086T>A (p.Ser696Thr)
c.1969T>A (p.Ser657Thr)
c.1510T>A (p.Ser504Thr)
c.1828T>A (p.Ser610Thr)
c.1492T>A (p.Ser498Thr)
n.75+5372A>T
6g.39357321T>ACA450098194KIF6c.2136A>T (p.Thr712=)
c.489A>T (p.Thr163=)
c.1811A>T
c.2085A>T (p.Thr695=)
c.1968A>T (p.Thr656=)
c.1509A>T (p.Thr503=)
c.1827A>T (p.Thr609=)
c.1491A>T (p.Thr497=)
n.75+5373T>A
6g.39357321T>CCA450098195KIF6c.2136A>G (p.Thr712=)
c.489A>G (p.Thr163=)
c.1811A>G
c.2085A>G (p.Thr695=)
c.1968A>G (p.Thr656=)
c.1509A>G (p.Thr503=)
c.1827A>G (p.Thr609=)
c.1491A>G (p.Thr497=)
n.75+5373T>C
6g.39357321T>GCA450098196KIF6c.2136A>C (p.Thr712=)
c.489A>C (p.Thr163=)
c.1811A>C
c.2085A>C (p.Thr695=)
c.1968A>C (p.Thr656=)
c.1509A>C (p.Thr503=)
c.1827A>C (p.Thr609=)
c.1491A>C (p.Thr497=)
n.75+5373T>G
6g.39357322G>ACA3793804KIF6c.2135C>T (p.Thr712Ile)
c.488C>T (p.Thr163Ile)
c.1810C>T
c.2084C>T (p.Thr695Ile)
c.1967C>T (p.Thr656Ile)
c.1508C>T (p.Thr503Ile)
c.1826C>T (p.Thr609Ile)
c.1490C>T (p.Thr497Ile)
n.75+5374G>A
dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357322G>CCA364350130KIF6c.2135C>G (p.Thr712Arg)
c.488C>G (p.Thr163Arg)
c.1810C>G
c.2084C>G (p.Thr695Arg)
c.1967C>G (p.Thr656Arg)
c.1508C>G (p.Thr503Arg)
c.1826C>G (p.Thr609Arg)
c.1490C>G (p.Thr497Arg)
n.75+5374G>C
6g.39357322G=CA1622646814KIF6c.2135C= (p.Thr712=)
c.488C= (p.Thr163=)
c.1810C=
c.2084C= (p.Thr695=)
c.1967C= (p.Thr656=)
c.1508C= (p.Thr503=)
c.1826C= (p.Thr609=)
c.1490C= (p.Thr497=)
n.75+5374G=
6g.39357322G>TCA364350131KIF6c.2135C>A (p.Thr712Lys)
c.488C>A (p.Thr163Lys)
c.1810C>A
c.2084C>A (p.Thr695Lys)
c.1967C>A (p.Thr656Lys)
c.1508C>A (p.Thr503Lys)
c.1826C>A (p.Thr609Lys)
c.1490C>A (p.Thr497Lys)
n.75+5374G>T
6g.39357323T>ACA364350133KIF6c.2134A>T (p.Thr712Ser)
c.487A>T (p.Thr163Ser)
c.1809A>T
c.2083A>T (p.Thr695Ser)
c.1966A>T (p.Thr656Ser)
c.1507A>T (p.Thr503Ser)
c.1825A>T (p.Thr609Ser)
c.1489A>T (p.Thr497Ser)
n.75+5375T>A

Number of alleles fetched