Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.40354427G>ACA438955540CHRNA9c.1347G>A (p.Lys449=)
dbSNP gnomAD v4
4g.40354427G>CCA356708053CHRNA9c.1347G>C (p.Lys449Asn)
4g.40354427G=CA1452584185CHRNA9c.1347G= (p.Lys449=)
4g.40354427G>TCA356708052CHRNA9c.1347G>T (p.Lys449Asn)
4g.40354428A>CCA356708057CHRNA9c.1348A>C (p.Lys450Gln)
4g.40354428A>GCA356708060CHRNA9c.1348A>G (p.Lys450Glu)
4g.40354428A>TCA356708062CHRNA9c.1348A>T (p.Lys450Ter)
4g.40354429A>CCA356708066CHRNA9c.1349A>C (p.Lys450Thr)
4g.40354429A>GCA356708069CHRNA9c.1349A>G (p.Lys450Arg)
4g.40354429A>TCA356708082CHRNA9c.1349A>T (p.Lys450Met)
4g.40354430G>ACA438955545CHRNA9c.1350G>A (p.Lys450=)
gnomAD v4
4g.40354430G>CCA356708096CHRNA9c.1350G>C (p.Lys450Asn)
4g.40354430G>TCA356708100CHRNA9c.1350G>T (p.Lys450Asn)
4g.40354431G>ACA356708105CHRNA9c.1351G>A (p.Val451Met)
4g.40354431G>CCA356708108CHRNA9c.1351G>C (p.Val451Leu)
4g.40354431G>TCA356708124CHRNA9c.1351G>T (p.Val451Leu)
4g.40354432T>ACA356708136CHRNA9c.1352T>A (p.Val451Glu)
4g.40354432T>CCA356708132CHRNA9c.1352T>C (p.Val451Ala)
dbSNP gnomAD v3 gnomAD v4
4g.40354432T>GCA356708128CHRNA9c.1352T>G (p.Val451Gly)
gnomAD v4
4g.40354432T=CA1452584188CHRNA9c.1352T= (p.Val451=)
4g.40354433G>ACA438955552CHRNA9c.1353G>A (p.Val451=)
gnomAD v4
4g.40354433G>CCA438955554CHRNA9c.1353G>C (p.Val451=)
4g.40354433G>TCA438955553CHRNA9c.1353G>T (p.Val451=)
4g.40354434G>ACA356708139CHRNA9c.1354G>A (p.Ala452Thr)
4g.40354434G>CCA356708142CHRNA9c.1354G>C (p.Ala452Pro)
4g.40354434G>TCA356708145CHRNA9c.1354G>T (p.Ala452Ser)
4g.40354435C>ACA356708148CHRNA9c.1355C>A (p.Ala452Glu)
dbSNP gnomAD v2 gnomAD v4
4g.40354435C=CA1452584465CHRNA9c.1355C= (p.Ala452=)
4g.40354435C>GCA356708150CHRNA9c.1355C>G (p.Ala452Gly)
4g.40354435C>TCA2898187CHRNA9c.1355C>T (p.Ala452Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.40354436G>ACA2898188CHRNA9c.1356G>A (p.Ala452=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.40354436G>CCA438955561CHRNA9c.1356G>C (p.Ala452=)
4g.40354436G=CA1452584479CHRNA9c.1356G= (p.Ala452=)
4g.40354436G>TCA438955562CHRNA9c.1356G>T (p.Ala452=)
dbSNP
4g.40354436_40354437delinsGACA1452584476CHRNA9c.1356_1357delinsGA (p.Ala452=)
4g.40354437A=CA1452584482CHRNA9c.1357A= (p.Lys453=)
4g.40354437A>CCA2898189CHRNA9c.1357A>C (p.Lys453Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.40354437A>GCA356708157CHRNA9c.1357A>G (p.Lys453Glu)
4g.40354437A>TCA356708159CHRNA9c.1357A>T (p.Lys453Ter)
4g.40354439delCA794768364CHRNA9c.1359del (p.Val454SerfsTer2)
dbSNP gnomAD v3 gnomAD v4
4g.40354438A>CCA356708163CHRNA9c.1358A>C (p.Lys453Thr)
4g.40354438A>GCA356708167CHRNA9c.1358A>G (p.Lys453Arg)
4g.40354438A>TCA356708174CHRNA9c.1358A>T (p.Lys453Ile)
4g.40354439A>CCA356708182CHRNA9c.1359A>C (p.Lys453Asn)
4g.40354439A>GCA438955568CHRNA9c.1359A>G (p.Lys453=)
4g.40354439A>TCA356708177CHRNA9c.1359A>T (p.Lys453Asn)
4g.40354440G>ACA356708185CHRNA9c.1360G>A (p.Val454Ile)
gnomAD v4
4g.40354440G>CCA356708187CHRNA9c.1360G>C (p.Val454Leu)
4g.40354440G>TCA356708189CHRNA9c.1360G>T (p.Val454Phe)
4g.40354441T>ACA356708194CHRNA9c.1361T>A (p.Val454Asp)

Number of alleles fetched