Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.61830406C>ACA222928955FADS2c.142-7372C>A (p.=)
c.115-7372C>A (p.=)
c.207+1809C>A (p.=)
c.-160+1809C>A (p.=)
c.-160+2975C>A (p.=)
dbSNP
11g.61830406C>TCA222928950FADS2c.142-7372C>T (p.=)
c.115-7372C>T (p.=)
c.207+1809C>T (p.=)
c.-160+1809C>T (p.=)
c.-160+2975C>T (p.=)
dbSNP
11g.61830411_61830413delCA679012460FADS2c.142-7367_142-7365del (p.=)
c.115-7367_115-7365del (p.=)
c.207+1814_207+1816del (p.=)
c.-160+1814_-160+1816del (p.=)
c.-160+2980_-160+2982del (p.=)
dbSNP
11g.61830413G>ACA599519813FADS2c.142-7365G>A (p.=)
c.115-7365G>A (p.=)
c.207+1816G>A (p.=)
c.-160+1816G>A (p.=)
c.-160+2982G>A (p.=)
gnomAD
11g.61830414T>ACA679012464FADS2c.142-7364T>A (p.=)
c.115-7364T>A (p.=)
c.207+1817T>A (p.=)
c.-160+1817T>A (p.=)
c.-160+2983T>A (p.=)
11g.61830416C>GCA222928961FADS2c.142-7362C>G (p.=)
c.115-7362C>G (p.=)
c.207+1819C>G (p.=)
c.-160+1819C>G (p.=)
c.-160+2985C>G (p.=)
dbSNP
11g.61830425C>TCA938619854FADS2c.142-7353C>T (p.=)
c.115-7353C>T (p.=)
c.207+1828C>T (p.=)
c.-160+1828C>T (p.=)
c.-160+2994C>T (p.=)
11g.61830426T>CCA938619861FADS2c.142-7352T>C (p.=)
c.115-7352T>C (p.=)
c.207+1829T>C (p.=)
c.-160+1829T>C (p.=)
c.-160+2995T>C (p.=)
11g.61830427C>TCA679012468FADS2c.142-7351C>T (p.=)
c.115-7351C>T (p.=)
c.207+1830C>T (p.=)
c.-160+1830C>T (p.=)
c.-160+2996C>T (p.=)
11g.61830433T>ACA222928973FADS2c.142-7345T>A (p.=)
c.115-7345T>A (p.=)
c.207+1836T>A (p.=)
c.-160+1836T>A (p.=)
c.-160+3002T>A (p.=)
dbSNP
11g.61830434T>CCA222928979FADS2c.142-7344T>C (p.=)
c.115-7344T>C (p.=)
c.207+1837T>C (p.=)
c.-160+1837T>C (p.=)
c.-160+3003T>C (p.=)
dbSNP
11g.61830435A>GCA599519815FADS2c.142-7343A>G (p.=)
c.115-7343A>G (p.=)
c.207+1838A>G (p.=)
c.-160+1838A>G (p.=)
c.-160+3004A>G (p.=)
gnomAD
11g.61830438T>CCA938619865FADS2c.142-7340T>C (p.=)
c.115-7340T>C (p.=)
c.207+1841T>C (p.=)
c.-160+1841T>C (p.=)
c.-160+3007T>C (p.=)
11g.61830441C>TCA222928993FADS2c.142-7337C>T (p.=)
c.115-7337C>T (p.=)
c.207+1844C>T (p.=)
c.-160+1844C>T (p.=)
c.-160+3010C>T (p.=)
dbSNP
11g.61830441delCA599519816FADS2c.142-7337del (p.=)
c.115-7337del (p.=)
c.207+1844del (p.=)
c.-160+1844del (p.=)
c.-160+3010del (p.=)
dbSNP gnomAD
11g.61830442C>TCA599519817FADS2c.142-7336C>T (p.=)
c.115-7336C>T (p.=)
c.207+1845C>T (p.=)
c.-160+1845C>T (p.=)
c.-160+3011C>T (p.=)
gnomAD
11g.61830448A>GCA222929000FADS2c.142-7330A>G (p.=)
c.115-7330A>G (p.=)
c.207+1851A>G (p.=)
c.-160+1851A>G (p.=)
c.-160+3017A>G (p.=)
dbSNP
11g.61830461C>TCA938619890FADS2c.142-7317C>T (p.=)
c.115-7317C>T (p.=)
c.207+1864C>T (p.=)
c.-160+1864C>T (p.=)
c.-160+3030C>T (p.=)
11g.61830465A>TCA938619891FADS2c.142-7313A>T (p.=)
c.115-7313A>T (p.=)
c.207+1868A>T (p.=)
c.-160+1868A>T (p.=)
c.-160+3034A>T (p.=)
11g.61830466A>GCA938619893FADS2c.142-7312A>G (p.=)
c.115-7312A>G (p.=)
c.207+1869A>G (p.=)
c.-160+1869A>G (p.=)
c.-160+3035A>G (p.=)
11g.61830469A>CCA679012486FADS2c.142-7309A>C (p.=)
c.115-7309A>C (p.=)
c.207+1872A>C (p.=)
c.-160+1872A>C (p.=)
c.-160+3038A>C (p.=)
11g.61830470G>ACA599519819FADS2c.142-7308G>A (p.=)
c.115-7308G>A (p.=)
c.207+1873G>A (p.=)
c.-160+1873G>A (p.=)
c.-160+3039G>A (p.=)
gnomAD
11g.61830473C>TCA599519820FADS2c.142-7305C>T (p.=)
c.115-7305C>T (p.=)
c.207+1876C>T (p.=)
c.-160+1876C>T (p.=)
c.-160+3042C>T (p.=)
gnomAD
11g.61830476A>CCA599519821FADS2c.142-7302A>C (p.=)
c.115-7302A>C (p.=)
c.207+1879A>C (p.=)
c.-160+1879A>C (p.=)
c.-160+3045A>C (p.=)
gnomAD
11g.61830478A>GCA599519822FADS2c.142-7300A>G (p.=)
c.115-7300A>G (p.=)
c.207+1881A>G (p.=)
c.-160+1881A>G (p.=)
c.-160+3047A>G (p.=)
gnomAD
11g.61830490_61830491delCA679012493FADS2c.142-7288_142-7287del (p.=)
c.115-7288_115-7287del (p.=)
c.207+1893_207+1894del (p.=)
c.-160+1893_-160+1894del (p.=)
c.-160+3059_-160+3060del (p.=)
dbSNP
11g.61830493G>ACA222929002FADS2c.142-7285G>A (p.=)
c.115-7285G>A (p.=)
c.207+1896G>A (p.=)
c.-160+1896G>A (p.=)
c.-160+3062G>A (p.=)
dbSNP
11g.61830493G>TCA679012496FADS2c.142-7285G>T (p.=)
c.115-7285G>T (p.=)
c.207+1896G>T (p.=)
c.-160+1896G>T (p.=)
c.-160+3062G>T (p.=)
11g.61830500A>GCA13485007FADS2c.142-7278A>G (p.=)
c.115-7278A>G (p.=)
c.207+1903A>G (p.=)
c.-160+1903A>G (p.=)
c.-160+3069A>G (p.=)
dbSNP gnomAD

Number of alleles fetched