Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.50319746G>ACA433691098HYAL2c.744C>T (p.Leu248=)
n.879C>T
dbSNP
3g.50319746G>CCA433691100HYAL2c.744C>G (p.Leu248=)
n.879C>G
3g.50319746G=CA1363891834HYAL2c.744C= (p.Leu248=)
n.879C=
3g.50319746G>TCA433691101HYAL2c.744C>A (p.Leu248=)
n.879C>A
3g.50319747A>CCA352907706HYAL2c.743T>G (p.Leu248Arg)
n.878T>G
3g.50319747A>GCA352907709HYAL2c.743T>C (p.Leu248Pro)
n.878T>C
3g.50319747A>TCA352907717HYAL2c.743T>A (p.Leu248His)
n.878T>A
3g.50319748G>ACA352909254HYAL2c.742C>T (p.Leu248Phe)
n.877C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.50319748G>CCA352909256HYAL2c.742C>G (p.Leu248Val)
n.877C>G
3g.50319748G=CA1363891837HYAL2c.742C= (p.Leu248=)
n.877C=
3g.50319748G>TCA352909259HYAL2c.742C>A (p.Leu248Ile)
n.877C>A
3g.50319749G>ACA433864272HYAL2c.741C>T (p.Ala247=)
n.876C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.50319749G>CCA433864273HYAL2c.741C>G (p.Ala247=)
n.876C>G
3g.50319749G=CA1363891840HYAL2c.741C= (p.Ala247=)
n.876C=
3g.50319749G>TCA433864274HYAL2c.741C>A (p.Ala247=)
n.876C>A
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

Number of alleles fetched