Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.39357331A=CA1622646818KIF6c.2126T= (p.Phe709=)
c.479T= (p.Phe160=)
c.1801T=
c.2075T= (p.Phe692=)
c.1958T= (p.Phe653=)
c.1499T= (p.Phe500=)
c.1817T= (p.Phe606=)
c.1481T= (p.Phe494=)
n.75+5383A=
6g.39357331A>CCA3793805KIF6c.2126T>G (p.Phe709Cys)
c.479T>G (p.Phe160Cys)
c.1801T>G
c.2075T>G (p.Phe692Cys)
c.1958T>G (p.Phe653Cys)
c.1499T>G (p.Phe500Cys)
c.1817T>G (p.Phe606Cys)
c.1481T>G (p.Phe494Cys)
n.75+5383A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357331A>GCA364350163KIF6c.2126T>C (p.Phe709Ser)
c.479T>C (p.Phe160Ser)
c.1801T>C
c.2075T>C (p.Phe692Ser)
c.1958T>C (p.Phe653Ser)
c.1499T>C (p.Phe500Ser)
c.1817T>C (p.Phe606Ser)
c.1481T>C (p.Phe494Ser)
n.75+5383A>G
6g.39357331A>TCA364350161KIF6c.2126T>A (p.Phe709Tyr)
c.479T>A (p.Phe160Tyr)
c.1801T>A
c.2075T>A (p.Phe692Tyr)
c.1958T>A (p.Phe653Tyr)
c.1499T>A (p.Phe500Tyr)
c.1817T>A (p.Phe606Tyr)
c.1481T>A (p.Phe494Tyr)
n.75+5383A>T
6g.39357332A>CCA364350166KIF6c.2125T>G (p.Phe709Val)
c.478T>G (p.Phe160Val)
c.1800T>G
c.2074T>G (p.Phe692Val)
c.1957T>G (p.Phe653Val)
c.1498T>G (p.Phe500Val)
c.1816T>G (p.Phe606Val)
c.1480T>G (p.Phe494Val)
n.75+5384A>C
6g.39357332A>GCA364350167KIF6c.2125T>C (p.Phe709Leu)
c.478T>C (p.Phe160Leu)
c.1800T>C
c.2074T>C (p.Phe692Leu)
c.1957T>C (p.Phe653Leu)
c.1498T>C (p.Phe500Leu)
c.1816T>C (p.Phe606Leu)
c.1480T>C (p.Phe494Leu)
n.75+5384A>G
 gnomAD v4
6g.39357332A>TCA364350168KIF6c.2125T>A (p.Phe709Ile)
c.478T>A (p.Phe160Ile)
c.1800T>A
c.2074T>A (p.Phe692Ile)
c.1957T>A (p.Phe653Ile)
c.1498T>A (p.Phe500Ile)
c.1816T>A (p.Phe606Ile)
c.1480T>A (p.Phe494Ile)
n.75+5384A>T
6g.39357333T>ACA450098202KIF6c.2124A>T (p.Pro708=)
c.477A>T (p.Pro159=)
c.1799A>T
c.2073A>T (p.Pro691=)
c.1956A>T (p.Pro652=)
c.1497A>T (p.Pro499=)
c.1815A>T (p.Pro605=)
c.1479A>T (p.Pro493=)
n.75+5385T>A
6g.39357333T>CCA450098203KIF6c.2124A>G (p.Pro708=)
c.477A>G (p.Pro159=)
c.1799A>G
c.2073A>G (p.Pro691=)
c.1956A>G (p.Pro652=)
c.1497A>G (p.Pro499=)
c.1815A>G (p.Pro605=)
c.1479A>G (p.Pro493=)
n.75+5385T>C
 dbSNP
6g.39357333T>GCA450098204KIF6c.2124A>C (p.Pro708=)
c.477A>C (p.Pro159=)
c.1799A>C
c.2073A>C (p.Pro691=)
c.1956A>C (p.Pro652=)
c.1497A>C (p.Pro499=)
c.1815A>C (p.Pro605=)
c.1479A>C (p.Pro493=)
n.75+5385T>G
6g.39357334G>ACA364350170KIF6c.2123C>T (p.Pro708Leu)
c.476C>T (p.Pro159Leu)
c.1798C>T
c.2072C>T (p.Pro691Leu)
c.1955C>T (p.Pro652Leu)
c.1496C>T (p.Pro499Leu)
c.1814C>T (p.Pro605Leu)
c.1478C>T (p.Pro493Leu)
n.75+5386G>A
 dbSNP gnomAD v3 gnomAD v4
6g.39357334G>CCA364350172KIF6c.2123C>G (p.Pro708Arg)
c.476C>G (p.Pro159Arg)
c.1798C>G
c.2072C>G (p.Pro691Arg)
c.1955C>G (p.Pro652Arg)
c.1496C>G (p.Pro499Arg)
c.1814C>G (p.Pro605Arg)
c.1478C>G (p.Pro493Arg)
n.75+5386G>C
6g.39357334G=CA1622646822KIF6c.2123C= (p.Pro708=)
c.476C= (p.Pro159=)
c.1798C=
c.2072C= (p.Pro691=)
c.1955C= (p.Pro652=)
c.1496C= (p.Pro499=)
c.1814C= (p.Pro605=)
c.1478C= (p.Pro493=)
n.75+5386G=
6g.39357334G>TCA364350174KIF6c.2123C>A (p.Pro708Gln)
c.476C>A (p.Pro159Gln)
c.1798C>A
c.2072C>A (p.Pro691Gln)
c.1955C>A (p.Pro652Gln)
c.1496C>A (p.Pro499Gln)
c.1814C>A (p.Pro605Gln)
c.1478C>A (p.Pro493Gln)
n.75+5386G>T
6g.39357335G>ACA3793806KIF6c.2122C>T (p.Pro708Ser)
c.475C>T (p.Pro159Ser)
c.1797C>T
c.2071C>T (p.Pro691Ser)
c.1954C>T (p.Pro652Ser)
c.1495C>T (p.Pro499Ser)
c.1813C>T (p.Pro605Ser)
c.1477C>T (p.Pro493Ser)
n.75+5387G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357335G>CCA364350175KIF6c.2122C>G (p.Pro708Ala)
c.475C>G (p.Pro159Ala)
c.1797C>G
c.2071C>G (p.Pro691Ala)
c.1954C>G (p.Pro652Ala)
c.1495C>G (p.Pro499Ala)
c.1813C>G (p.Pro605Ala)
c.1477C>G (p.Pro493Ala)
n.75+5387G>C
6g.39357335G=CA1622646827KIF6c.2122C= (p.Pro708=)
c.475C= (p.Pro159=)
c.1797C=
c.2071C= (p.Pro691=)
c.1954C= (p.Pro652=)
c.1495C= (p.Pro499=)
c.1813C= (p.Pro605=)
c.1477C= (p.Pro493=)
n.75+5387G=
6g.39357335G>TCA3793807KIF6c.2122C>A (p.Pro708Thr)
c.475C>A (p.Pro159Thr)
c.1797C>A
c.2071C>A (p.Pro691Thr)
c.1954C>A (p.Pro652Thr)
c.1495C>A (p.Pro499Thr)
c.1813C>A (p.Pro605Thr)
c.1477C>A (p.Pro493Thr)
n.75+5387G>T
 dbSNP ExAC gnomAD v4
6g.39357336C>ACA364350178KIF6c.2121G>T (p.Lys707Asn)
c.474G>T (p.Lys158Asn)
c.1796G>T
c.2070G>T (p.Lys690Asn)
c.1953G>T (p.Lys651Asn)
c.1494G>T (p.Lys498Asn)
c.1812G>T (p.Lys604Asn)
c.1476G>T (p.Lys492Asn)
n.75+5388C>A
6g.39357336C>GCA364350179KIF6c.2121G>C (p.Lys707Asn)
c.474G>C (p.Lys158Asn)
c.1796G>C
c.2070G>C (p.Lys690Asn)
c.1953G>C (p.Lys651Asn)
c.1494G>C (p.Lys498Asn)
c.1812G>C (p.Lys604Asn)
c.1476G>C (p.Lys492Asn)
n.75+5388C>G
6g.39357336C>TCA450098205KIF6c.2121G>A (p.Lys707=)
c.474G>A (p.Lys158=)
c.1796G>A
c.2070G>A (p.Lys690=)
c.1953G>A (p.Lys651=)
c.1494G>A (p.Lys498=)
c.1812G>A (p.Lys604=)
c.1476G>A (p.Lys492=)
n.75+5388C>T
6g.39357337T>ACA364350183KIF6c.2120A>T (p.Lys707Met)
c.473A>T (p.Lys158Met)
c.1795A>T
c.2069A>T (p.Lys690Met)
c.1952A>T (p.Lys651Met)
c.1493A>T (p.Lys498Met)
c.1811A>T (p.Lys604Met)
c.1475A>T (p.Lys492Met)
n.75+5389T>A
6g.39357337T>CCA364350182KIF6c.2120A>G (p.Lys707Arg)
c.473A>G (p.Lys158Arg)
c.1795A>G
c.2069A>G (p.Lys690Arg)
c.1952A>G (p.Lys651Arg)
c.1493A>G (p.Lys498Arg)
c.1811A>G (p.Lys604Arg)
c.1475A>G (p.Lys492Arg)
n.75+5389T>C
6g.39357337T>GCA364350181KIF6c.2120A>C (p.Lys707Thr)
c.473A>C (p.Lys158Thr)
c.1795A>C
c.2069A>C (p.Lys690Thr)
c.1952A>C (p.Lys651Thr)
c.1493A>C (p.Lys498Thr)
c.1811A>C (p.Lys604Thr)
c.1475A>C (p.Lys492Thr)
n.75+5389T>G
6g.39357338T>ACA364350184KIF6c.2119A>T (p.Lys707Ter)
c.472A>T (p.Lys158Ter)
c.1794A>T
c.2068A>T (p.Lys690Ter)
c.1951A>T (p.Lys651Ter)
c.1492A>T (p.Lys498Ter)
c.1810A>T (p.Lys604Ter)
c.1474A>T (p.Lys492Ter)
n.75+5390T>A
6g.39357338T>CCA364350185KIF6c.2119A>G (p.Lys707Glu)
c.472A>G (p.Lys158Glu)
c.1794A>G
c.2068A>G (p.Lys690Glu)
c.1951A>G (p.Lys651Glu)
c.1492A>G (p.Lys498Glu)
c.1810A>G (p.Lys604Glu)
c.1474A>G (p.Lys492Glu)
n.75+5390T>C
6g.39357338T>GCA364350186KIF6c.2119A>C (p.Lys707Gln)
c.472A>C (p.Lys158Gln)
c.1794A>C
c.2068A>C (p.Lys690Gln)
c.1951A>C (p.Lys651Gln)
c.1492A>C (p.Lys498Gln)
c.1810A>C (p.Lys604Gln)
c.1474A>C (p.Lys492Gln)
n.75+5390T>G
6g.39357339C>ACA450098206KIF6c.2118G>T (p.Thr706=)
c.471G>T (p.Thr157=)
c.1793G>T
c.2067G>T (p.Thr689=)
c.1950G>T (p.Thr650=)
c.1491G>T (p.Thr497=)
c.1809G>T (p.Thr603=)
c.1473G>T (p.Thr491=)
n.75+5391C>A
6g.39357339C=CA1622646830KIF6c.2118G= (p.Thr706=)
c.471G= (p.Thr157=)
c.1793G=
c.2067G= (p.Thr689=)
c.1950G= (p.Thr650=)
c.1491G= (p.Thr497=)
c.1809G= (p.Thr603=)
c.1473G= (p.Thr491=)
n.75+5391C=
6g.39357339C>GCA450098207KIF6c.2118G>C (p.Thr706=)
c.471G>C (p.Thr157=)
c.1793G>C
c.2067G>C (p.Thr689=)
c.1950G>C (p.Thr650=)
c.1491G>C (p.Thr497=)
c.1809G>C (p.Thr603=)
c.1473G>C (p.Thr491=)
n.75+5391C>G
6g.39357339C>TCA3793808KIF6c.2118G>A (p.Thr706=)
c.471G>A (p.Thr157=)
c.1793G>A
c.2067G>A (p.Thr689=)
c.1950G>A (p.Thr650=)
c.1491G>A (p.Thr497=)
c.1809G>A (p.Thr603=)
c.1473G>A (p.Thr491=)
n.75+5391C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.39357340G>ACA3793809KIF6c.2117C>T (p.Thr706Met)
c.470C>T (p.Thr157Met)
c.1792C>T
c.2066C>T (p.Thr689Met)
c.1949C>T (p.Thr650Met)
c.1490C>T (p.Thr497Met)
c.1808C>T (p.Thr603Met)
c.1472C>T (p.Thr491Met)
n.75+5392G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.39357340G>CCA3793810KIF6c.2117C>G (p.Thr706Arg)
c.470C>G (p.Thr157Arg)
c.1792C>G
c.2066C>G (p.Thr689Arg)
c.1949C>G (p.Thr650Arg)
c.1490C>G (p.Thr497Arg)
c.1808C>G (p.Thr603Arg)
c.1472C>G (p.Thr491Arg)
n.75+5392G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.39357340G=CA1622646832KIF6c.2117C= (p.Thr706=)
c.470C= (p.Thr157=)
c.1792C=
c.2066C= (p.Thr689=)
c.1949C= (p.Thr650=)
c.1490C= (p.Thr497=)
c.1808C= (p.Thr603=)
c.1472C= (p.Thr491=)
n.75+5392G=
6g.39357340G>TCA364350190KIF6c.2117C>A (p.Thr706Lys)
c.470C>A (p.Thr157Lys)
c.1792C>A
c.2066C>A (p.Thr689Lys)
c.1949C>A (p.Thr650Lys)
c.1490C>A (p.Thr497Lys)
c.1808C>A (p.Thr603Lys)
c.1472C>A (p.Thr491Lys)
n.75+5392G>T
6g.39357341T>ACA364350195KIF6c.2116A>T (p.Thr706Ser)
c.469A>T (p.Thr157Ser)
c.1791A>T
c.2065A>T (p.Thr689Ser)
c.1948A>T (p.Thr650Ser)
c.1489A>T (p.Thr497Ser)
c.1807A>T (p.Thr603Ser)
c.1471A>T (p.Thr491Ser)
n.75+5393T>A
6g.39357341T>CCA364350191KIF6c.2116A>G (p.Thr706Ala)
c.469A>G (p.Thr157Ala)
c.1791A>G
c.2065A>G (p.Thr689Ala)
c.1948A>G (p.Thr650Ala)
c.1489A>G (p.Thr497Ala)
c.1807A>G (p.Thr603Ala)
c.1471A>G (p.Thr491Ala)
n.75+5393T>C
6g.39357341T>GCA364350193KIF6c.2116A>C (p.Thr706Pro)
c.469A>C (p.Thr157Pro)
c.1791A>C
c.2065A>C (p.Thr689Pro)
c.1948A>C (p.Thr650Pro)
c.1489A>C (p.Thr497Pro)
c.1807A>C (p.Thr603Pro)
c.1471A>C (p.Thr491Pro)
n.75+5393T>G
6g.39357342G>ACA450098208KIF6c.2115C>T (p.His705=)
c.468C>T (p.His156=)
c.1790C>T
c.2064C>T (p.His688=)
c.1947C>T (p.His649=)
c.1488C>T (p.His496=)
c.1806C>T (p.His602=)
c.1470C>T (p.His490=)
n.75+5394G>A
6g.39357342G>CCA364350196KIF6c.2115C>G (p.His705Gln)
c.468C>G (p.His156Gln)
c.1790C>G
c.2064C>G (p.His688Gln)
c.1947C>G (p.His649Gln)
c.1488C>G (p.His496Gln)
c.1806C>G (p.His602Gln)
c.1470C>G (p.His490Gln)
n.75+5394G>C
6g.39357342G>TCA364350198KIF6c.2115C>A (p.His705Gln)
c.468C>A (p.His156Gln)
c.1790C>A
c.2064C>A (p.His688Gln)
c.1947C>A (p.His649Gln)
c.1488C>A (p.His496Gln)
c.1806C>A (p.His602Gln)
c.1470C>A (p.His490Gln)
n.75+5394G>T
6g.39357343T>ACA364350200KIF6c.2114A>T (p.His705Leu)
c.467A>T (p.His156Leu)
c.1789A>T
c.2063A>T (p.His688Leu)
c.1946A>T (p.His649Leu)
c.1487A>T (p.His496Leu)
c.1805A>T (p.His602Leu)
c.1469A>T (p.His490Leu)
n.75+5395T>A
6g.39357343T>CCA364350202KIF6c.2114A>G (p.His705Arg)
c.467A>G (p.His156Arg)
c.1789A>G
c.2063A>G (p.His688Arg)
c.1946A>G (p.His649Arg)
c.1487A>G (p.His496Arg)
c.1805A>G (p.His602Arg)
c.1469A>G (p.His490Arg)
n.75+5395T>C
6g.39357343T>GCA364350203KIF6c.2114A>C (p.His705Pro)
c.467A>C (p.His156Pro)
c.1789A>C
c.2063A>C (p.His688Pro)
c.1946A>C (p.His649Pro)
c.1487A>C (p.His496Pro)
c.1805A>C (p.His602Pro)
c.1469A>C (p.His490Pro)
n.75+5395T>G
6g.39357344G>ACA364350205KIF6c.2113C>T (p.His705Tyr)
c.466C>T (p.His156Tyr)
c.1788C>T
c.2062C>T (p.His688Tyr)
c.1945C>T (p.His649Tyr)
c.1486C>T (p.His496Tyr)
c.1804C>T (p.His602Tyr)
c.1468C>T (p.His490Tyr)
n.75+5396G>A
6g.39357344G>CCA364350208KIF6c.2113C>G (p.His705Asp)
c.466C>G (p.His156Asp)
c.1788C>G
c.2062C>G (p.His688Asp)
c.1945C>G (p.His649Asp)
c.1486C>G (p.His496Asp)
c.1804C>G (p.His602Asp)
c.1468C>G (p.His490Asp)
n.75+5396G>C
6g.39357344G>TCA364350207KIF6c.2113C>A (p.His705Asn)
c.466C>A (p.His156Asn)
c.1788C>A
c.2062C>A (p.His688Asn)
c.1945C>A (p.His649Asn)
c.1486C>A (p.His496Asn)
c.1804C>A (p.His602Asn)
c.1468C>A (p.His490Asn)
n.75+5396G>T
6g.39357345A>CCA364350210KIF6c.2112T>G (p.Asp704Glu)
c.465T>G (p.Asp155Glu)
c.1787T>G
c.2061T>G (p.Asp687Glu)
c.1944T>G (p.Asp648Glu)
c.1485T>G (p.Asp495Glu)
c.1803T>G (p.Asp601Glu)
c.1467T>G (p.Asp489Glu)
n.75+5397A>C
6g.39357345A>GCA450098209KIF6c.2112T>C (p.Asp704=)
c.465T>C (p.Asp155=)
c.1787T>C
c.2061T>C (p.Asp687=)
c.1944T>C (p.Asp648=)
c.1485T>C (p.Asp495=)
c.1803T>C (p.Asp601=)
c.1467T>C (p.Asp489=)
n.75+5397A>G
 gnomAD v4
6g.39357345A>TCA364350211KIF6c.2112T>A (p.Asp704Glu)
c.465T>A (p.Asp155Glu)
c.1787T>A
c.2061T>A (p.Asp687Glu)
c.1944T>A (p.Asp648Glu)
c.1485T>A (p.Asp495Glu)
c.1803T>A (p.Asp601Glu)
c.1467T>A (p.Asp489Glu)
n.75+5397A>T

Number of alleles fetched