Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.97450069A>CCA341375920DPYDc.1895T>G (p.Phe632Cys)
c.1679T>G (p.Phe560Cys)
c.1784T>G (p.Phe595Cys)
c.1400T>G (p.Phe467Cys)
1g.97450069A>GCA341375921DPYDc.1895T>C (p.Phe632Ser)
c.1679T>C (p.Phe560Ser)
c.1784T>C (p.Phe595Ser)
c.1400T>C (p.Phe467Ser)
gnomAD v4
1g.97450069A>TCA341375922DPYDc.1895T>A (p.Phe632Tyr)
c.1679T>A (p.Phe560Tyr)
c.1784T>A (p.Phe595Tyr)
c.1400T>A (p.Phe467Tyr)
1g.97450070A>CCA341375923DPYDc.1894T>G (p.Phe632Val)
c.1678T>G (p.Phe560Val)
c.1783T>G (p.Phe595Val)
c.1399T>G (p.Phe467Val)
1g.97450070A>GCA341375924DPYDc.1894T>C (p.Phe632Leu)
c.1678T>C (p.Phe560Leu)
c.1783T>C (p.Phe595Leu)
c.1399T>C (p.Phe467Leu)
1g.97450070A>TCA341375925DPYDc.1894T>A (p.Phe632Ile)
c.1678T>A (p.Phe560Ile)
c.1783T>A (p.Phe595Ile)
c.1399T>A (p.Phe467Ile)
dbSNP
1g.97450071G>ACA27501722DPYDc.1893C>T (p.Asp631=)
c.1677C>T (p.Asp559=)
c.1782C>T (p.Asp594=)
c.1398C>T (p.Asp466=)
dbSNP gnomAD v4
1g.97450071G>CCA341375926DPYDc.1893C>G (p.Asp631Glu)
c.1677C>G (p.Asp559Glu)
c.1782C>G (p.Asp594Glu)
c.1398C>G (p.Asp466Glu)
dbSNP COSMIC
1g.97450071G=CA1182873431DPYDc.1893C= (p.Asp631=)
c.1677C= (p.Asp559=)
c.1782C= (p.Asp594=)
c.1398C= (p.Asp466=)
1g.97450071G>TCA341375927DPYDc.1893C>A (p.Asp631Glu)
c.1677C>A (p.Asp559Glu)
c.1782C>A (p.Asp594Glu)
c.1398C>A (p.Asp466Glu)
COSMIC
1g.97450072T>ACA341375928DPYDc.1892A>T (p.Asp631Val)
c.1676A>T (p.Asp559Val)
c.1781A>T (p.Asp594Val)
c.1397A>T (p.Asp466Val)
dbSNP
1g.97450072T>CCA341375930DPYDc.1892A>G (p.Asp631Gly)
c.1676A>G (p.Asp559Gly)
c.1781A>G (p.Asp594Gly)
c.1397A>G (p.Asp466Gly)
1g.97450072T>GCA341375929DPYDc.1892A>C (p.Asp631Ala)
c.1676A>C (p.Asp559Ala)
c.1781A>C (p.Asp594Ala)
c.1397A>C (p.Asp466Ala)
dbSNP
1g.97450073C>ACA341375931DPYDc.1891G>T (p.Asp631Tyr)
c.1675G>T (p.Asp559Tyr)
c.1780G>T (p.Asp594Tyr)
c.1396G>T (p.Asp466Tyr)
dbSNP
1g.97450073C=CA1182873432DPYDc.1891G= (p.Asp631=)
c.1675G= (p.Asp559=)
c.1780G= (p.Asp594=)
c.1396G= (p.Asp466=)
1g.97450073C>GCA341375932DPYDc.1891G>C (p.Asp631His)
c.1675G>C (p.Asp559His)
c.1780G>C (p.Asp594His)
c.1396G>C (p.Asp466His)
dbSNP
1g.97450073C>TCA341375933DPYDc.1891G>A (p.Asp631Asn)
c.1675G>A (p.Asp559Asn)
c.1780G>A (p.Asp594Asn)
c.1396G>A (p.Asp466Asn)
dbSNP
1g.97450074A>CCA419145351DPYDc.1890T>G (p.Ala630=)
c.1674T>G (p.Ala558=)
c.1779T>G (p.Ala593=)
c.1395T>G (p.Ala465=)
1g.97450074A>GCA419145352DPYDc.1890T>C (p.Ala630=)
c.1674T>C (p.Ala558=)
c.1779T>C (p.Ala593=)
c.1395T>C (p.Ala465=)
dbSNP
1g.97450074A>TCA419145353DPYDc.1890T>A (p.Ala630=)
c.1674T>A (p.Ala558=)
c.1779T>A (p.Ala593=)
c.1395T>A (p.Ala465=)
dbSNP
1g.97450075G>ACA341375934DPYDc.1889C>T (p.Ala630Val)
c.1673C>T (p.Ala558Val)
c.1778C>T (p.Ala593Val)
c.1394C>T (p.Ala465Val)
dbSNP
1g.97450075G>CCA341375935DPYDc.1889C>G (p.Ala630Gly)
c.1673C>G (p.Ala558Gly)
c.1778C>G (p.Ala593Gly)
c.1394C>G (p.Ala465Gly)
dbSNP
1g.97450075G=CA1182873433DPYDc.1889C= (p.Ala630=)
c.1673C= (p.Ala558=)
c.1778C= (p.Ala593=)
c.1394C= (p.Ala465=)
1g.97450075G>TCA341375936DPYDc.1889C>A (p.Ala630Asp)
c.1673C>A (p.Ala558Asp)
c.1778C>A (p.Ala593Asp)
c.1394C>A (p.Ala465Asp)
1g.97450076C>ACA341375937DPYDc.1888G>T (p.Ala630Ser)
c.1672G>T (p.Ala558Ser)
c.1777G>T (p.Ala593Ser)
c.1393G>T (p.Ala465Ser)
dbSNP
1g.97450076C=CA1182873434DPYDc.1888G= (p.Ala630=)
c.1672G= (p.Ala558=)
c.1777G= (p.Ala593=)
c.1393G= (p.Ala465=)
1g.97450076C>GCA341375938DPYDc.1888G>C (p.Ala630Pro)
c.1672G>C (p.Ala558Pro)
c.1777G>C (p.Ala593Pro)
c.1393G>C (p.Ala465Pro)
dbSNP
1g.97450076C>TCA341375939DPYDc.1888G>A (p.Ala630Thr)
c.1672G>A (p.Ala558Thr)
c.1777G>A (p.Ala593Thr)
c.1393G>A (p.Ala465Thr)
dbSNP
1g.97450077C>ACA341375940DPYDc.1887G>T (p.Lys629Asn)
c.1671G>T (p.Lys557Asn)
c.1776G>T (p.Lys592Asn)
c.1392G>T (p.Lys464Asn)
COSMIC
1g.97450077C>GCA341375941DPYDc.1887G>C (p.Lys629Asn)
c.1671G>C (p.Lys557Asn)
c.1776G>C (p.Lys592Asn)
c.1392G>C (p.Lys464Asn)
1g.97450077C>TCA419145357DPYDc.1887G>A (p.Lys629=)
c.1671G>A (p.Lys557=)
c.1776G>A (p.Lys592=)
c.1392G>A (p.Lys464=)
1g.97450078T>ACA341375944DPYDc.1886A>T (p.Lys629Met)
c.1670A>T (p.Lys557Met)
c.1775A>T (p.Lys592Met)
c.1391A>T (p.Lys464Met)
dbSNP gnomAD v4
1g.97450078T>CCA341375942DPYDc.1886A>G (p.Lys629Arg)
c.1670A>G (p.Lys557Arg)
c.1775A>G (p.Lys592Arg)
c.1391A>G (p.Lys464Arg)
1g.97450078T>GCA341375943DPYDc.1886A>C (p.Lys629Thr)
c.1670A>C (p.Lys557Thr)
c.1775A>C (p.Lys592Thr)
c.1391A>C (p.Lys464Thr)
1g.97450079T>ACA341375945DPYDc.1885A>T (p.Lys629Ter)
c.1669A>T (p.Lys557Ter)
c.1774A>T (p.Lys592Ter)
c.1390A>T (p.Lys464Ter)
1g.97450079T>CCA341375946DPYDc.1885A>G (p.Lys629Glu)
c.1669A>G (p.Lys557Glu)
c.1774A>G (p.Lys592Glu)
c.1390A>G (p.Lys464Glu)
1g.97450079T>GCA341375947DPYDc.1885A>C (p.Lys629Gln)
c.1669A>C (p.Lys557Gln)
c.1774A>C (p.Lys592Gln)
c.1390A>C (p.Lys464Gln)
1g.97450080T>ACA419145360DPYDc.1884A>T (p.Leu628=)
c.1668A>T (p.Leu556=)
c.1773A>T (p.Leu591=)
c.1389A>T (p.Leu463=)
1g.97450080T>CCA419145361DPYDc.1884A>G (p.Leu628=)
c.1668A>G (p.Leu556=)
c.1773A>G (p.Leu591=)
c.1389A>G (p.Leu463=)
gnomAD v4
1g.97450080T>GCA419145362DPYDc.1884A>C (p.Leu628=)
c.1668A>C (p.Leu556=)
c.1773A>C (p.Leu591=)
c.1389A>C (p.Leu463=)
1g.97450081A>CCA341375948DPYDc.1883T>G (p.Leu628Arg)
c.1667T>G (p.Leu556Arg)
c.1772T>G (p.Leu591Arg)
c.1388T>G (p.Leu463Arg)
1g.97450081A>GCA341375949DPYDc.1883T>C (p.Leu628Pro)
c.1667T>C (p.Leu556Pro)
c.1772T>C (p.Leu591Pro)
c.1388T>C (p.Leu463Pro)
gnomAD v4
1g.97450081A>TCA341375950DPYDc.1883T>A (p.Leu628Gln)
c.1667T>A (p.Leu556Gln)
c.1772T>A (p.Leu591Gln)
c.1388T>A (p.Leu463Gln)
dbSNP
1g.97450082G>ACA27501723DPYDc.1882C>T (p.Leu628=)
c.1666C>T (p.Leu556=)
c.1771C>T (p.Leu591=)
c.1387C>T (p.Leu463=)
dbSNP
1g.97450082G>CCA341375951DPYDc.1882C>G (p.Leu628Val)
c.1666C>G (p.Leu556Val)
c.1771C>G (p.Leu591Val)
c.1387C>G (p.Leu463Val)
dbSNP
1g.97450082G=CA1182873435DPYDc.1882C= (p.Leu628=)
c.1666C= (p.Leu556=)
c.1771C= (p.Leu591=)
c.1387C= (p.Leu463=)
1g.97450082G>TCA341375952DPYDc.1882C>A (p.Leu628Ile)
c.1666C>A (p.Leu556Ile)
c.1771C>A (p.Leu591Ile)
c.1387C>A (p.Leu463Ile)
1g.97450083T>ACA341375953DPYDc.1881A>T (p.Glu627Asp)
c.1665A>T (p.Glu555Asp)
c.1770A>T (p.Glu590Asp)
c.1386A>T (p.Glu462Asp)
1g.97450083T>CCA419145364DPYDc.1881A>G (p.Glu627=)
c.1665A>G (p.Glu555=)
c.1770A>G (p.Glu590=)
c.1386A>G (p.Glu462=)
1g.97450083T>GCA341375954DPYDc.1881A>C (p.Glu627Asp)
c.1665A>C (p.Glu555Asp)
c.1770A>C (p.Glu590Asp)
c.1386A>C (p.Glu462Asp)

Number of alleles fetched