Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.19957641delCA849561489LPLc.1018+1558del (p.=)
n.79+1558del (p.=)
dbSNP
8g.19957644T>GCA849561493LPLc.1018+1561T>G (p.=)
n.79+1561T>G (p.=)
8g.19957644T=CA1769106714LPLc.1018+1561T= (p.=)
n.79+1561T= (p.=)
8g.19957649T>ACA173378989LPLc.1018+1566T>A (p.=)
n.79+1566T>A (p.=)
dbSNP
8g.19957649T=CA1769106718LPLc.1018+1566T= (p.=)
n.79+1566T= (p.=)
8g.19957650C>ACA1769106724LPLc.1018+1567C>A (p.=)
n.79+1567C>A (p.=)
8g.19957650C=CA1769106722LPLc.1018+1567C= (p.=)
n.79+1567C= (p.=)
8g.19957653A=CA1769106726LPLc.1018+1570A= (p.=)
n.79+1570A= (p.=)
8g.19957653A>TCA1769106727LPLc.1018+1570A>T (p.=)
n.79+1570A>T (p.=)
8g.19957656T>CCA1111553167LPLc.1018+1573T>C (p.=)
n.79+1573T>C (p.=)
8g.19957656T=CA1769106729LPLc.1018+1573T= (p.=)
n.79+1573T= (p.=)
8g.19957658A=CA1769106733LPLc.1018+1575A= (p.=)
n.79+1575A= (p.=)
8g.19957658A>GCA173378991LPLc.1018+1575A>G (p.=)
n.79+1575A>G (p.=)
dbSNP
8g.19957659A=CA1769106735LPLc.1018+1576A= (p.=)
n.79+1576A= (p.=)
8g.19957659A>GCA580158097LPLc.1018+1576A>G (p.=)
n.79+1576A>G (p.=)
gnomAD
8g.19957660T>CCA1769106738LPLc.1018+1577T>C (p.=)
n.79+1577T>C (p.=)
8g.19957660T=CA1769106737LPLc.1018+1577T= (p.=)
n.79+1577T= (p.=)
8g.19957661G>ACA1111553169LPLc.1018+1578G>A (p.=)
n.79+1578G>A (p.=)
8g.19957661G=CA1769106740LPLc.1018+1578G= (p.=)
n.79+1578G= (p.=)
8g.19957663C>ACA173378994LPLc.1018+1580C>A (p.=)
n.79+1580C>A (p.=)
dbSNP
8g.19957663C=CA1769106744LPLc.1018+1580C= (p.=)
n.79+1580C= (p.=)
8g.19957663C>GCA1111553171LPLc.1018+1580C>G (p.=)
n.79+1580C>G (p.=)
8g.19957663C>TCA1111553176LPLc.1018+1580C>T (p.=)
n.79+1580C>T (p.=)
8g.19957667T>CCA1769106746LPLc.1018+1584T>C (p.=)
n.79+1584T>C (p.=)
8g.19957667T=CA1769106747LPLc.1018+1584T= (p.=)
n.79+1584T= (p.=)
8g.19957668C=CA1769106749LPLc.1018+1585C= (p.=)
n.79+1585C= (p.=)
8g.19957668C>TCA1769106752LPLc.1018+1585C>T (p.=)
n.79+1585C>T (p.=)
8g.19957671C=CA1769106755LPLc.1019-1589C= (p.=)
n.79+1588C= (p.=)
8g.19957674_19957675dupCA580158100LPLc.1019-1586_1019-1585dup (p.=)
n.79+1591_79+1592dup (p.=)
dbSNP gnomAD
8g.19957674T>CCA1111553186LPLc.1019-1586T>C (p.=)
n.79+1591T>C (p.=)
8g.19957674T=CA1769106759LPLc.1019-1586T= (p.=)
n.79+1591T= (p.=)
8g.19957678C=CA1769106761LPLc.1019-1582C= (p.=)
n.79+1595C= (p.=)
8g.19957678C>GCA1769106763LPLc.1019-1582C>G (p.=)
n.79+1595C>G (p.=)
8g.19957678C>TCA15543537LPLc.1019-1582C>T (p.=)
n.79+1595C>T (p.=)
dbSNP gnomAD
8g.19957680G>ACA1769106769LPLc.1019-1580G>A (p.=)
n.79+1597G>A (p.=)
8g.19957680G=CA1769106767LPLc.1019-1580G= (p.=)
n.79+1597G= (p.=)
8g.19957681C=CA1769106773LPLc.1019-1579C= (p.=)
n.79+1598C= (p.=)
8g.19957681C>TCA849561501LPLc.1019-1579C>T (p.=)
n.79+1598C>T (p.=)
8g.19957682T>ACA652181296LPLc.1019-1578T>A (p.=)
n.79+1599T>A (p.=)
COSMIC
8g.19957684T>CCA1769106781LPLc.1019-1576T>C (p.=)
n.79+1601T>C (p.=)
8g.19957684T=CA1769106778LPLc.1019-1576T= (p.=)
n.79+1601T= (p.=)
8g.19957685G=CA1769106786LPLc.1019-1575G= (p.=)
n.79+1602G= (p.=)
8g.19957685G>TCA173378998LPLc.1019-1575G>T (p.=)
n.79+1602G>T (p.=)
dbSNP
8g.19957687G>CCA173379000LPLc.1019-1573G>C (p.=)
n.79+1604G>C (p.=)
dbSNP
8g.19957687G=CA1769106787LPLc.1019-1573G= (p.=)
n.79+1604G= (p.=)
8g.19957690_19957693delinsTTTGCA1769106790LPLc.1019-1570_1019-1567delinsTTTG (p.=)
n.79+1607_79+1610delinsTTTG (p.=)
8g.19957699_19957701delCA1769106792LPLc.1019-1561_1019-1559del (p.=)
n.79+1616_79+1618del (p.=)
dbSNP
8g.19957692T>CCA849561504LPLc.1019-1568T>C (p.=)
n.79+1609T>C (p.=)
8g.19957692T=CA1769106793LPLc.1019-1568T= (p.=)
n.79+1609T= (p.=)
8g.19957694T>CCA849561510LPLc.1019-1566T>C (p.=)
n.79+1611T>C (p.=)
gnomAD

Number of alleles fetched