Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.69035772_69035877delCA2690187648FXNc.-11_95del
gnomAD v4
9g.69035807G>ACA373527279FXNc.25G>A (p.Val9Ile)
c.23G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.69035807G>CCA373527280FXNc.25G>C (p.Val9Leu)
c.23G>C
gnomAD v4
9g.69035807G=CA1854034927FXNc.25G= (p.Val9=)
c.23G=
9g.69035807G>TCA373527278FXNc.25G>T (p.Val9Leu)
c.23G>T
gnomAD v4
9g.69035808T>ACA373527283FXNc.26T>A (p.Val9Glu)
c.24T>A
9g.69035808T>CCA373527281FXNc.26T>C (p.Val9Ala)
c.24T>C
gnomAD v4
9g.69035808T>GCA373527282FXNc.26T>G (p.Val9Gly)
c.24T>G
9g.69035809A=CA1854034928FXNc.27A= (p.Val9=)
c.25A=
9g.69035809A>CCA465233036FXNc.27A>C (p.Val9=)
c.25A>C
9g.69035809A>GCA465233038FXNc.27A>G (p.Val9=)
c.25A>G
dbSNP
9g.69035809A>TCA465233040FXNc.27A>T (p.Val9=)
c.25A>T
9g.69035810G>ACA193368950FXNc.28G>A (p.Ala10Thr)
c.26G>A
dbSNP
9g.69035810G>CCA373527284FXNc.28G>C (p.Ala10Pro)
c.26G>C
9g.69035810G=CA1854034929FXNc.28G= (p.Ala10=)
c.26G=
9g.69035810G>TCA373527285FXNc.28G>T (p.Ala10Ser)
c.26G>T
gnomAD v4
9g.69035811C>ACA373527288FXNc.29C>A (p.Ala10Asp)
c.27C>A
gnomAD v4
9g.69035811C=CA1854034930FXNc.29C= (p.Ala10=)
c.27C=
9g.69035811C>GCA373527287FXNc.29C>G (p.Ala10Gly)
c.27C>G
9g.69035811C>TCA373527286FXNc.29C>T (p.Ala10Val)
c.27C>T
dbSNP gnomAD v3 gnomAD v4
9g.69035812C>ACA465233053FXNc.30C>A (p.Ala10=)
c.28C>A
dbSNP gnomAD v4
9g.69035812C=CA1854034931FXNc.30C= (p.Ala10=)
c.28C=
9g.69035812C>GCA465233051FXNc.30C>G (p.Ala10=)
c.28C>G
gnomAD v4
9g.69035812C>TCA193368957FXNc.30C>T (p.Ala10=)
c.28C>T
dbSNP gnomAD v2 gnomAD v4
9g.69035813G>ACA373527289FXNc.31G>A (p.Gly11Ser)
c.29G>A
dbSNP gnomAD v4
9g.69035813G>CCA373527290FXNc.31G>C (p.Gly11Arg)
c.29G>C
9g.69035813G=CA1854034932FXNc.31G= (p.Gly11=)
c.29G=
9g.69035813G>TCA373527291FXNc.31G>T (p.Gly11Cys)
c.29G>T
gnomAD v4
9g.69035814G>ACA373527292FXNc.32G>A (p.Gly11Asp)
c.30G>A
gnomAD v4
9g.69035814G>CCA373527293FXNc.32G>C (p.Gly11Ala)
c.30G>C
9g.69035814G=CA1854034933FXNc.32G= (p.Gly11=)
c.30G=
9g.69035814G>TCA373527294FXNc.32G>T (p.Gly11Val)
c.30G>T
dbSNP gnomAD v2 gnomAD v4
9g.69035815C>ACA465233065FXNc.33C>A (p.Gly11=)
c.31C>A
gnomAD v4
9g.69035815C=CA1854034934FXNc.33C= (p.Gly11=)
c.31C=
9g.69035815C>GCA465233069FXNc.33C>G (p.Gly11=)
c.31C>G
9g.69035815C>TCA465233067FXNc.33C>T (p.Gly11=)
c.31C>T
dbSNP gnomAD v2 gnomAD v4
9g.69035816C>ACA373527295FXNc.34C>A (p.Leu12Ile)
c.32C>A
dbSNP gnomAD v2 gnomAD v4
9g.69035816C=CA1854034935FXNc.34C= (p.Leu12=)
c.32C=
9g.69035816C>GCA373527297FXNc.34C>G (p.Leu12Val)
c.32C>G
ClinVar dbSNP gnomAD v4
9g.69035816C>TCA373527296FXNc.34C>T (p.Leu12Phe)
c.32C>T
9g.69035817T>ACA373527298FXNc.35T>A (p.Leu12His)
c.33T>A
9g.69035817T>CCA373527299FXNc.35T>C (p.Leu12Pro)
c.33T>C
gnomAD v4
9g.69035817T>GCA373527300FXNc.35T>G (p.Leu12Arg)
c.33T>G
9g.69035818C>ACA465233079FXNc.36C>A (p.Leu12=)
c.34C>A
gnomAD v4
9g.69035818C=CA1854034936FXNc.36C= (p.Leu12=)
c.34C=
9g.69035818C>GCA465233083FXNc.36C>G (p.Leu12=)
c.34C>G
9g.69035818C>TCA465233081FXNc.36C>T (p.Leu12=)
c.34C>T
dbSNP gnomAD v2 gnomAD v4
9g.69035819C>ACA373527301FXNc.37C>A (p.Leu13Met)
c.35C>A
9g.69035819C>GCA373527302FXNc.37C>G (p.Leu13Val)
c.35C>G
9g.69035819C>TCA465233087FXNc.37C>T (p.Leu13=)
c.35C>T
gnomAD v4

Number of alleles fetched