Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.50319750G>ACA352909269HYAL2c.740C>T (p.Ala247Val)
n.875C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.50319750G>CCA352909262HYAL2c.740C>G (p.Ala247Gly)
n.875C>G
3g.50319750G=CA1363891843HYAL2c.740C= (p.Ala247=)
n.875C=
3g.50319750G>TCA352909264HYAL2c.740C>A (p.Ala247Asp)
n.875C>A
3g.50319751C>ACA352909272HYAL2c.739G>T (p.Ala247Ser)
n.874G>T
dbSNP gnomAD v4
3g.50319751C=CA1363891846HYAL2c.739G= (p.Ala247=)
n.874G=
3g.50319751C>GCA352909275HYAL2c.739G>C (p.Ala247Pro)
n.874G>C
3g.50319751C>TCA352909277HYAL2c.739G>A (p.Ala247Thr)
n.874G>A
dbSNP
3g.50319752C>ACA2416246HYAL2c.738G>T (p.Thr246=)
n.873G>T
dbSNP ExAC gnomAD v2 gnomAD v4
3g.50319752C=CA1363891848HYAL2c.738G= (p.Thr246=)
n.873G=
3g.50319752C>GCA433864284HYAL2c.738G>C (p.Thr246=)
n.873G>C
gnomAD v4
3g.50319752C>TCA2416245HYAL2c.738G>A (p.Thr246=)
n.873G>A
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.50319753G>ACA2416247HYAL2c.737C>T (p.Thr246Met)
n.872C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.50319753G>CCA352909285HYAL2c.737C>G (p.Thr246Arg)
n.872C>G
3g.50319753G=CA1363891850HYAL2c.737C= (p.Thr246=)
n.872C=
3g.50319753G>TCA352909288HYAL2c.737C>A (p.Thr246Lys)
n.872C>A
3g.50319754T>ACA352909292HYAL2c.736A>T (p.Thr246Ser)
n.871A>T
3g.50319754T>CCA352909294HYAL2c.736A>G (p.Thr246Ala)
n.871A>G
dbSNP gnomAD v2 gnomAD v4
3g.50319754T>GCA352909297HYAL2c.736A>C (p.Thr246Pro)
n.871A>C
3g.50319754T=CA1363891853HYAL2c.736A= (p.Thr246=)
n.871A=
3g.50319755G>ACA433864290HYAL2c.735C>T (p.Ser245=)
n.870C>T
3g.50319755G>CCA352909300HYAL2c.735C>G (p.Ser245Arg)
n.870C>G
3g.50319755G>TCA352909303HYAL2c.735C>A (p.Ser245Arg)
n.870C>A
3g.50319756C>ACA352909305HYAL2c.734G>T (p.Ser245Ile)
n.869G>T
3g.50319756C=CA1363891855HYAL2c.734G= (p.Ser245=)
n.869G=
3g.50319756C>GCA352909308HYAL2c.734G>C (p.Ser245Thr)
n.869G>C
3g.50319756C>TCA2416248HYAL2c.734G>A (p.Ser245Asn)
n.869G>A
dbSNP ExAC gnomAD v2 gnomAD v4
3g.50319757T>ACA352909311HYAL2c.733A>T (p.Ser245Cys)
n.868A>T
3g.50319757T>CCA352909313HYAL2c.733A>G (p.Ser245Gly)
n.868A>G
3g.50319757T>GCA352909316HYAL2c.733A>C (p.Ser245Arg)
n.868A>C
3g.50319758C>ACA352909319HYAL2c.732G>T (p.Glu244Asp)
n.867G>T
3g.50319758C=CA1363891857HYAL2c.732G= (p.Glu244=)
n.867G=
3g.50319758C>GCA74612591HYAL2c.732G>C (p.Glu244Asp)
n.867G>C
dbSNP gnomAD v2 gnomAD v4
3g.50319758C>TCA433864294HYAL2c.732G>A (p.Glu244=)
n.867G>A
dbSNP gnomAD v2 gnomAD v4
3g.50319759T>ACA352909324HYAL2c.731A>T (p.Glu244Val)
n.866A>T
3g.50319759T>CCA352909326HYAL2c.731A>G (p.Glu244Gly)
n.866A>G
gnomAD v4
3g.50319759T>GCA352909325HYAL2c.731A>C (p.Glu244Ala)
n.866A>C
3g.50319760C>ACA352909327HYAL2c.730G>T (p.Glu244Ter)
n.865G>T
3g.50319760C>GCA352909330HYAL2c.730G>C (p.Glu244Gln)
n.865G>C
gnomAD v4
3g.50319760C>TCA352909333HYAL2c.730G>A (p.Glu244Lys)
n.865G>A
COSMIC
3g.50319761A>CCA433864297HYAL2c.729T>G (p.Ala243=)
n.864T>G
3g.50319761A>GCA433864298HYAL2c.729T>C (p.Ala243=)
n.864T>C
3g.50319761A>TCA433864299HYAL2c.729T>A (p.Ala243=)
n.864T>A
3g.50319762G>ACA352909335HYAL2c.728C>T (p.Ala243Val)
n.863C>T
3g.50319762G>CCA352909337HYAL2c.728C>G (p.Ala243Gly)
n.863C>G
dbSNP gnomAD v3 gnomAD v4
3g.50319762G=CA1363891859HYAL2c.728C= (p.Ala243=)
n.863C=
3g.50319762G>TCA352909340HYAL2c.728C>A (p.Ala243Asp)
n.863C>A
3g.50319763C>ACA352909342HYAL2c.727G>T (p.Ala243Ser)
n.862G>T
3g.50319763C=CA1363891861HYAL2c.727G= (p.Ala243=)
n.862G=
3g.50319763C>GCA352909345HYAL2c.727G>C (p.Ala243Pro)
n.862G>C

Number of alleles fetched