Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.50319647G>ACA433690717HYAL2c.843C>T (p.Thr281=)
n.978C>T
3g.50319647G>CCA433690721HYAL2c.843C>G (p.Thr281=)
n.978C>G
3g.50319647G=CA1363891751HYAL2c.843C= (p.Thr281=)
n.978C=
3g.50319647G>TCA433690723HYAL2c.843C>A (p.Thr281=)
n.978C>A
dbSNP
3g.50319647_50319648insACCA2756211177HYAL2c.842_843insGT (p.His282SerfsTer?)
n.977_978insGT
3g.50319648G>ACA352907039HYAL2c.842C>T (p.Thr281Ile)
n.977C>T
gnomAD v4
3g.50319648G>CCA352907037HYAL2c.842C>G (p.Thr281Ser)
n.977C>G
gnomAD v4
3g.50319648G>TCA352907034HYAL2c.842C>A (p.Thr281Asn)
n.977C>A
3g.50319649T>ACA352907041HYAL2c.841A>T (p.Thr281Ser)
n.976A>T
3g.50319649T>CCA352907044HYAL2c.841A>G (p.Thr281Ala)
n.976A>G
3g.50319649T>GCA352907048HYAL2c.841A>C (p.Thr281Pro)
n.976A>C
dbSNP
3g.50319649T=CA1363891752HYAL2c.841A= (p.Thr281=)
n.976A=
3g.50319650delCA2756211178HYAL2c.840del (p.Thr281ProfsTer?)
n.975del
3g.50319650G>ACA433690731HYAL2c.840C>T (p.Arg280=)
n.975C>T
3g.50319650G>CCA433690732HYAL2c.840C>G (p.Arg280=)
n.975C>G
3g.50319650G>TCA433690733HYAL2c.840C>A (p.Arg280=)
n.975C>A
3g.50319651C>ACA352907053HYAL2c.839G>T (p.Arg280Leu)
n.974G>T
gnomAD v4
3g.50319651C=CA1363891753HYAL2c.839G= (p.Arg280=)
n.974G=
3g.50319651C>GCA2416224HYAL2c.839G>C (p.Arg280Pro)
n.974G>C
dbSNP ExAC gnomAD v4
3g.50319651C>TCA2416223HYAL2c.839G>A (p.Arg280His)
n.974G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.50319652delCA2756211179HYAL2c.838del (p.Arg280AlafsTer?)
n.973del
3g.50319652G>ACA2416225HYAL2c.838C>T (p.Arg280Cys)
n.973C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.50319652G>CCA352907059HYAL2c.838C>G (p.Arg280Gly)
n.973C>G
dbSNP
3g.50319652G=CA1363891754HYAL2c.838C= (p.Arg280=)
n.973C=
3g.50319652G>TCA352907062HYAL2c.838C>A (p.Arg280Ser)
n.973C>A
3g.50319653A>CCA433690747HYAL2c.837T>G (p.Ala279=)
n.972T>G
3g.50319653A>GCA433690748HYAL2c.837T>C (p.Ala279=)
n.972T>C
gnomAD v4
3g.50319653A>TCA433690749HYAL2c.837T>A (p.Ala279=)
n.972T>A
3g.50319654G>ACA352907066HYAL2c.836C>T (p.Ala279Val)
n.971C>T
3g.50319654G>CCA352907068HYAL2c.836C>G (p.Ala279Gly)
n.971C>G
gnomAD v4
3g.50319654G>TCA352907072HYAL2c.836C>A (p.Ala279Asp)
n.971C>A
3g.50319655C>ACA352907078HYAL2c.835G>T (p.Ala279Ser)
n.970G>T
3g.50319655C>GCA352907076HYAL2c.835G>C (p.Ala279Pro)
n.970G>C
3g.50319655C>TCA352907075HYAL2c.835G>A (p.Ala279Thr)
n.970G>A
3g.50319656C>ACA433690759HYAL2c.834G>T (p.Val278=)
n.969G>T
3g.50319656C>GCA433690760HYAL2c.834G>C (p.Val278=)
n.969G>C
3g.50319656C>TCA433690762HYAL2c.834G>A (p.Val278=)
n.969G>A
3g.50319657A>CCA352907081HYAL2c.833T>G (p.Val278Gly)
n.968T>G
3g.50319657A>GCA352907083HYAL2c.833T>C (p.Val278Ala)
n.968T>C
3g.50319657A>TCA352907086HYAL2c.833T>A (p.Val278Glu)
n.968T>A
3g.50319658C>ACA352907088HYAL2c.832G>T (p.Val278Leu)
n.967G>T
3g.50319658C>GCA352907093HYAL2c.832G>C (p.Val278Leu)
n.967G>C
3g.50319658C>TCA352907096HYAL2c.832G>A (p.Val278Met)
n.967G>A
3g.50319659A=CA1363891755HYAL2c.831T= (p.Arg277=)
n.966T=
3g.50319659A>CCA433690770HYAL2c.831T>G (p.Arg277=)
n.966T>G
3g.50319659A>GCA433690768HYAL2c.831T>C (p.Arg277=)
n.966T>C
dbSNP gnomAD v3 gnomAD v4
3g.50319659A>TCA433690766HYAL2c.831T>A (p.Arg277=)
n.966T>A
3g.50319660C>ACA352907099HYAL2c.830G>T (p.Arg277Leu)
n.965G>T
gnomAD v4
3g.50319660C=CA1363891756HYAL2c.830G= (p.Arg277=)
n.965G=
3g.50319660C>GCA352907101HYAL2c.830G>C (p.Arg277Pro)
n.965G>C

Number of alleles fetched