Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.33443327delCA2577372685SNTA1c.296del (p.Gly99AlafsTer?)
n.529del
gnomAD v4
20g.33443325_33443335delCA2816180525SNTA1c.286_296del (p.Gly96HisfsTer25)
n.519_529del
20g.33443327C>ACA510252397SNTA1c.294G>T (p.Leu98=)
n.527G>T
gnomAD v4
20g.33443327C>GCA510252396SNTA1c.294G>C (p.Leu98=)
n.527G>C
gnomAD v4
20g.33443327C>TCA510252395SNTA1c.294G>A (p.Leu98=)
n.527G>A
gnomAD v4
20g.33443328A>CCA408633906SNTA1c.293T>G (p.Leu98Arg)
n.526T>G
20g.33443328A>GCA408633909SNTA1c.293T>C (p.Leu98Pro)
n.526T>C
gnomAD v4
20g.33443328A>TCA408633908SNTA1c.293T>A (p.Leu98Gln)
n.526T>A
gnomAD v4
20g.33443329G>ACA510252398SNTA1c.292C>T (p.Leu98=)
n.525C>T
ClinVar dbSNP gnomAD v4
20g.33443329G>CCA408633911SNTA1c.292C>G (p.Leu98Val)
n.525C>G
gnomAD v4
20g.33443329G>TCA408633912SNTA1c.292C>A (p.Leu98Met)
n.525C>A
gnomAD v4
20g.33443330C>ACA510252399SNTA1c.291G>T (p.Gly97=)
n.524G>T
gnomAD v4
20g.33443330C>GCA510252400SNTA1c.291G>C (p.Gly97=)
n.524G>C
20g.33443330C>TCA510252401SNTA1c.291G>A (p.Gly97=)
n.524G>A
gnomAD v4
20g.33443332delCA2652478365SNTA1c.291del (p.Leu98TrpfsTer?)
n.524del
gnomAD v4
20g.33443331C>ACA408633914SNTA1c.290G>T (p.Gly97Val)
n.523G>T
gnomAD v4
20g.33443331C>GCA408633915SNTA1c.290G>C (p.Gly97Ala)
n.523G>C
20g.33443331C>TCA408633916SNTA1c.290G>A (p.Gly97Glu)
n.523G>A
gnomAD v4
20g.33443332C>ACA408633917SNTA1c.289G>T (p.Gly97Trp)
n.522G>T
gnomAD v4
20g.33443332C=CA2360754884SNTA1c.289G= (p.Gly97=)
n.522G=
20g.33443332C>GCA9817261SNTA1c.289G>C (p.Gly97Arg)
n.522G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.33443332C>TCA408633919SNTA1c.289G>A (p.Gly97Arg)
n.522G>A
gnomAD v4
20g.33443333A>CCA510252402SNTA1c.288T>G (p.Gly96=)
n.521T>G
20g.33443333A>GCA510252403SNTA1c.288T>C (p.Gly96=)
n.521T>C
gnomAD v4
20g.33443333A>TCA510252404SNTA1c.288T>A (p.Gly96=)
n.521T>A
20g.33443334C>ACA408633921SNTA1c.287G>T (p.Gly96Val)
n.520G>T
gnomAD v4
20g.33443334C=CA2360754885SNTA1c.287G= (p.Gly96=)
n.520G=
20g.33443334C>GCA302252SNTA1c.287G>C (p.Gly96Ala)
n.520G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.33443334C>TCA408633923SNTA1c.287G>A (p.Gly96Asp)
n.520G>A
gnomAD v4
20g.33443335C>ACA408633925SNTA1c.286G>T (p.Gly96Cys)
n.519G>T
gnomAD v4
20g.33443335C=CA2360754886SNTA1c.286G= (p.Gly96=)
n.519G=
20g.33443335C>GCA408633926SNTA1c.286G>C (p.Gly96Arg)
n.519G>C
gnomAD v4
20g.33443335C>TCA313278884SNTA1c.286G>A (p.Gly96Ser)
n.519G>A
ClinVar dbSNP gnomAD v4
20g.33443336G>ACA510252405SNTA1c.285C>T (p.Ala95=)
n.518C>T
gnomAD v4
20g.33443336G>CCA510252406SNTA1c.285C>G (p.Ala95=)
n.518C>G
gnomAD v4
20g.33443336G>TCA510252407SNTA1c.285C>A (p.Ala95=)
n.518C>A
gnomAD v4
20g.33443337G>ACA408633932SNTA1c.284C>T (p.Ala95Val)
n.517C>T
gnomAD v4
20g.33443337G>CCA408633930SNTA1c.284C>G (p.Ala95Gly)
n.517C>G
dbSNP gnomAD v4
20g.33443337G=CA2360754887SNTA1c.284C= (p.Ala95=)
n.517C=
20g.33443337G>TCA408633929SNTA1c.284C>A (p.Ala95Asp)
n.517C>A
gnomAD v4
20g.33443338C>ACA408633933SNTA1c.283G>T (p.Ala95Ser)
n.516G>T
gnomAD v4
20g.33443338C>GCA408633934SNTA1c.283G>C (p.Ala95Pro)
n.516G>C
20g.33443338C>TCA408633937SNTA1c.283G>A (p.Ala95Thr)
n.516G>A
gnomAD v4
20g.33443339G>ACA510252408SNTA1c.282C>T (p.Asp94=)
n.515C>T
gnomAD v4
20g.33443339G>CCA408633939SNTA1c.282C>G (p.Asp94Glu)
n.515C>G
gnomAD v4
20g.33443339G>TCA408633940SNTA1c.282C>A (p.Asp94Glu)
n.515C>A
gnomAD v4
20g.33443340T>ACA408633942SNTA1c.281A>T (p.Asp94Val)
n.514A>T
20g.33443340T>CCA408633943SNTA1c.281A>G (p.Asp94Gly)
n.514A>G
gnomAD v4
20g.33443340T>GCA408633945SNTA1c.281A>C (p.Asp94Ala)
n.514A>C
dbSNP gnomAD v2 gnomAD v4
20g.33443340T=CA2360754888SNTA1c.281A= (p.Asp94=)
n.514A=

Number of alleles fetched