Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.26480783_26480805dupCA1239827691OTOFc.1786_1803+5dup
c.1831_1848+5dup
dbSNP gnomAD v4
2g.26480784A>CCA346132514OTOFc.1803+2T>G (n.1803+2T>G)
c.1848+2T>G (n.1848+2T>G)
2g.26480784A>GCA346132517OTOFc.1803+2T>C (n.1803+2T>C)
c.1848+2T>C (n.1848+2T>C)
2g.26480784A>TCA346132519OTOFc.1803+2T>A (n.1803+2T>A)
c.1848+2T>A (n.1848+2T>A)
2g.26480784_26480785delinsACCA1239827694OTOFc.1803+1_1803+2delinsGT (n.1803+1_1803+2delinsGT)
c.1848+1_1848+2delinsGT (n.1848+1_1848+2delinsGT)
2g.26480785C>ACA346132521OTOFc.1803+1G>T (n.1803+1G>T)
c.1848+1G>T (n.1848+1G>T)
2g.26480785C>GCA346132523OTOFc.1803+1G>C (n.1803+1G>C)
c.1848+1G>C (n.1848+1G>C)
2g.26480785C>TCA346132526OTOFc.1803+1G>A (n.1803+1G>A)
c.1848+1G>A (n.1848+1G>A)
ClinVar dbSNP gnomAD v4
2g.26480786delCA767288499OTOFc.1803+1del
c.1848+1del
dbSNP gnomAD v3 gnomAD v4
2g.26480786C>ACA346132528OTOFc.1803G>T (p.Glu601Asp)
c.1848G>T (p.Glu616Asp)
2g.26480786C>GCA346132530OTOFc.1803G>C (p.Glu601Asp)
c.1848G>C (p.Glu616Asp)
2g.26480786C>TCA425205810OTOFc.1803G>A (p.Glu601=)
c.1848G>A (p.Glu616=)
gnomAD v4
2g.26480787T>ACA346132533OTOFc.1802A>T (p.Glu601Val)
c.1847A>T (p.Glu616Val)
2g.26480787T>CCA346132535OTOFc.1802A>G (p.Glu601Gly)
c.1847A>G (p.Glu616Gly)
2g.26480787T>GCA346132536OTOFc.1802A>C (p.Glu601Ala)
c.1847A>C (p.Glu616Ala)
2g.26480788C>ACA346132538OTOFc.1801G>T (p.Glu601Ter)
c.1846G>T (p.Glu616Ter)
ClinVar dbSNP
2g.26480788C=CA1239827696OTOFc.1801G= (p.Glu601=)
c.1846G= (p.Glu616=)
2g.26480788C>GCA346132540OTOFc.1801G>C (p.Glu601Gln)
c.1846G>C (p.Glu616Gln)
2g.26480788C>TCA346132542OTOFc.1801G>A (p.Glu601Lys)
c.1846G>A (p.Glu616Lys)
COSMIC
2g.26480789C>ACA425205818OTOFc.1800G>T (p.Ser600=)
c.1845G>T (p.Ser615=)
gnomAD v4
2g.26480789C=CA1239827697OTOFc.1800G= (p.Ser600=)
c.1845G= (p.Ser615=)
2g.26480789C>GCA425205820OTOFc.1800G>C (p.Ser600=)
c.1845G>C (p.Ser615=)
2g.26480789C>TCA142764OTOFc.1800G>A (p.Ser600=)
c.1845G>A (p.Ser615=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.26480790G>ACA1564179OTOFc.1799C>T (p.Ser600Leu)
c.1844C>T (p.Ser615Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.26480790G>CCA346132548OTOFc.1799C>G (p.Ser600Trp)
c.1844C>G (p.Ser615Trp)
2g.26480790G=CA1239827700OTOFc.1799C= (p.Ser600=)
c.1844C= (p.Ser615=)
2g.26480790G>TCA346132551OTOFc.1799C>A (p.Ser600Ter)
c.1844C>A (p.Ser615Ter)
dbSNP gnomAD v4
2g.26480791A=CA1239827702OTOFc.1798T= (p.Ser600=)
c.1843T= (p.Ser615=)
2g.26480791A>CCA346132554OTOFc.1798T>G (p.Ser600Ala)
c.1843T>G (p.Ser615Ala)
2g.26480791A>GCA346132556OTOFc.1798T>C (p.Ser600Pro)
c.1843T>C (p.Ser615Pro)
dbSNP gnomAD v2 gnomAD v4
2g.26480791A>TCA346132558OTOFc.1798T>A (p.Ser600Thr)
c.1843T>A (p.Ser615Thr)
2g.26480792G>ACA425205827OTOFc.1797C>T (p.Ile599=)
c.1842C>T (p.Ile614=)
2g.26480792G>CCA346132560OTOFc.1797C>G (p.Ile599Met)
c.1842C>G (p.Ile614Met)
2g.26480792G>TCA425205831OTOFc.1797C>A (p.Ile599=)
c.1842C>A (p.Ile614=)
2g.26480793A>CCA346132568OTOFc.1796T>G (p.Ile599Ser)
c.1841T>G (p.Ile614Ser)
2g.26480793A>GCA346132564OTOFc.1796T>C (p.Ile599Thr)
c.1841T>C (p.Ile614Thr)
2g.26480793A>TCA346132567OTOFc.1796T>A (p.Ile599Asn)
c.1841T>A (p.Ile614Asn)
2g.26480794T>ACA1564180OTOFc.1795A>T (p.Ile599Phe)
c.1840A>T (p.Ile614Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.26480794T>CCA346132569OTOFc.1795A>G (p.Ile599Val)
c.1840A>G (p.Ile614Val)
2g.26480794T>GCA346132570OTOFc.1795A>C (p.Ile599Leu)
c.1840A>C (p.Ile614Leu)
gnomAD v4
2g.26480794T=CA1239827703OTOFc.1795A= (p.Ile599=)
c.1840A= (p.Ile614=)
2g.26480795G>ACA425205834OTOFc.1794C>T (p.Pro598=)
c.1839C>T (p.Pro613=)
gnomAD v4
2g.26480795G>CCA425205835OTOFc.1794C>G (p.Pro598=)
c.1839C>G (p.Pro613=)
gnomAD v4
2g.26480795G>TCA425205836OTOFc.1794C>A (p.Pro598=)
c.1839C>A (p.Pro613=)
gnomAD v4
2g.26480796G>ACA346132573OTOFc.1793C>T (p.Pro598Leu)
c.1838C>T (p.Pro613Leu)
2g.26480796G>CCA346132575OTOFc.1793C>G (p.Pro598Arg)
c.1838C>G (p.Pro613Arg)
2g.26480796G>TCA346132577OTOFc.1793C>A (p.Pro598His)
c.1838C>A (p.Pro613His)
2g.26480797G>ACA346132580OTOFc.1792C>T (p.Pro598Ser)
c.1837C>T (p.Pro613Ser)
gnomAD v4
2g.26480797G>CCA346132585OTOFc.1792C>G (p.Pro598Ala)
c.1837C>G (p.Pro613Ala)
2g.26480797G=CA1239827705OTOFc.1792C= (p.Pro598=)
c.1837C= (p.Pro613=)

Number of alleles fetched