Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.33879324C=CA1538170418ADAMTS12c.489+1795G= (n.489+1795G=)
5g.33879324C>TCA810022890ADAMTS12c.489+1795G>A (n.489+1795G>A)
dbSNP
5g.33879329C>TCA2708397720ADAMTS12c.489+1790G>A (n.489+1790G>A)
dbSNP
5g.33879331G>CCA1074896384ADAMTS12c.489+1788C>G (n.489+1788C>G)
dbSNP gnomAD v3 gnomAD v4
5g.33879331G=CA1538170419ADAMTS12c.489+1788C= (n.489+1788C=)
5g.33879332C=CA1538170420ADAMTS12c.489+1787G= (n.489+1787G=)
5g.33879332C>TCA1538170421ADAMTS12c.489+1787G>A (n.489+1787G>A)
dbSNP
5g.33879335C=CA1538170422ADAMTS12c.489+1784G= (n.489+1784G=)
5g.33879335C>TCA1538170423ADAMTS12c.489+1784G>A (n.489+1784G>A)
dbSNP
5g.33879339C=CA1538170424ADAMTS12c.489+1780G= (n.489+1780G=)
5g.33879339C>GCA1538170425ADAMTS12c.489+1780G>C (n.489+1780G>C)
dbSNP
5g.33879343G>ACA2595111070ADAMTS12c.489+1776C>T (n.489+1776C>T)
gnomAD v3 gnomAD v4
5g.33879343G>CCA1538170427ADAMTS12c.489+1776C>G (n.489+1776C>G)
dbSNP
5g.33879343G=CA1538170426ADAMTS12c.489+1776C= (n.489+1776C=)
5g.33879345A=CA1538170428ADAMTS12c.489+1774T= (n.489+1774T=)
5g.33879345A>GCA117271040ADAMTS12c.489+1774T>C (n.489+1774T>C)
dbSNP
5g.33879349A=CA1538170429ADAMTS12c.489+1770T= (n.489+1770T=)
5g.33879349A>GCA810022892ADAMTS12c.489+1770T>C (n.489+1770T>C)
dbSNP
5g.33879352C=CA1538170430ADAMTS12c.489+1767G= (n.489+1767G=)
5g.33879352C>TCA117271041ADAMTS12c.489+1767G>A (n.489+1767G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.33879354C>ACA2528439213ADAMTS12c.489+1765G>T (n.489+1765G>T)
5g.33879354C>TCA2708397744ADAMTS12c.489+1765G>A (n.489+1765G>A)
dbSNP
5g.33879355A=CA1538170431ADAMTS12c.489+1764T= (n.489+1764T=)
5g.33879355A>CCA1538170432ADAMTS12c.489+1764T>G (n.489+1764T>G)
dbSNP
5g.33879356T>CCA810022896ADAMTS12c.489+1763A>G (n.489+1763A>G)
dbSNP
5g.33879356T>GCA1538170434ADAMTS12c.489+1763A>C (n.489+1763A>C)
dbSNP
5g.33879356T=CA1538170433ADAMTS12c.489+1763A= (n.489+1763A=)
5g.33879363T>CCA1074896385ADAMTS12c.489+1756A>G (n.489+1756A>G)
dbSNP gnomAD v3 gnomAD v4
5g.33879363T>GCA1538170436ADAMTS12c.489+1756A>C (n.489+1756A>C)
dbSNP
5g.33879363T=CA1538170435ADAMTS12c.489+1756A= (n.489+1756A=)
5g.33879364G>ACA1538170438ADAMTS12c.489+1755C>T (n.489+1755C>T)
dbSNP
5g.33879364G=CA1538170437ADAMTS12c.489+1755C= (n.489+1755C=)
5g.33879367C>ACA2533396933ADAMTS12c.489+1752G>T (n.489+1752G>T)
5g.33879368A=CA1538170439ADAMTS12c.489+1751T= (n.489+1751T=)
5g.33879368A>TCA117271042ADAMTS12c.489+1751T>A (n.489+1751T>A)
dbSNP
5g.33879376G=CA1538170440ADAMTS12c.489+1743C= (n.489+1743C=)
5g.33879376G>TCA117271043ADAMTS12c.489+1743C>A (n.489+1743C>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.33879385T>CCA1538170442ADAMTS12c.489+1734A>G (n.489+1734A>G)
dbSNP
5g.33879385T=CA1538170441ADAMTS12c.489+1734A= (n.489+1734A=)
5g.33879387C=CA1538170443ADAMTS12c.489+1732G= (n.489+1732G=)
5g.33879387C>TCA1538170444ADAMTS12c.489+1732G>A (n.489+1732G>A)
dbSNP
5g.33879388A=CA1538170445ADAMTS12c.489+1731T= (n.489+1731T=)
5g.33879388A>CCA1538170446ADAMTS12c.489+1731T>G (n.489+1731T>G)
dbSNP
5g.33879391A=CA1538170447ADAMTS12c.489+1728T= (n.489+1728T=)
5g.33879391A>CCA117271044ADAMTS12c.489+1728T>G (n.489+1728T>G)
dbSNP gnomAD v3 gnomAD v4
5g.33879392C>ACA810022899ADAMTS12c.489+1727G>T (n.489+1727G>T)
dbSNP
5g.33879392C=CA1538170448ADAMTS12c.489+1727G= (n.489+1727G=)
5g.33879392C>TCA1074896389ADAMTS12c.489+1727G>A (n.489+1727G>A)
dbSNP gnomAD v3 gnomAD v4
5g.33879399C=CA1538170449ADAMTS12c.489+1720G= (n.489+1720G=)
5g.33879399C>TCA117271045ADAMTS12c.489+1720G>A (n.489+1720G>A)
dbSNP gnomAD v3 gnomAD v4
5g.33879407G>ACA1538170450ADAMTS12c.489+1712C>T (n.489+1712C>T)
dbSNP
5g.33879407G=CA1538170451ADAMTS12c.489+1712C= (n.489+1712C=)
5g.33879411T>CCA810022906ADAMTS12c.489+1708A>G (n.489+1708A>G)
dbSNP
5g.33879411T=CA1538170452ADAMTS12c.489+1708A= (n.489+1708A=)
5g.33879413G>ACA810022912ADAMTS12c.489+1706C>T (n.489+1706C>T)
dbSNP
5g.33879413G=CA1538170453ADAMTS12c.489+1706C= (n.489+1706C=)
5g.33879416G>ACA117271046ADAMTS12c.489+1703C>T (n.489+1703C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.33879416G>CCA2595111072ADAMTS12c.489+1703C>G (n.489+1703C>G)
dbSNP gnomAD v3 gnomAD v4
5g.33879416G=CA1538170454ADAMTS12c.489+1703C= (n.489+1703C=)
5g.33879416G>TCA1538170455ADAMTS12c.489+1703C>A (n.489+1703C>A)
dbSNP
5g.33879419C=CA1538170456ADAMTS12c.489+1700G= (n.489+1700G=)
5g.33879419C>TCA117271047ADAMTS12c.489+1700G>A (n.489+1700G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched