Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50624902C>TCA1026679981ARSAc.*243G>A (p.=)
22g.50624905C>TCA325531071ARSAc.*240G>A (p.=)
dbSNP
22g.50624909C>ACA1026679988ARSAc.*236G>T (p.=)
22g.50624909C>TCA325531073ARSAc.*236G>A (p.=)
dbSNP gnomAD
22g.50624911_50624915delCA754067036ARSAc.*228_*232del (p.=)
dbSNP
22g.50624913C>GCA325531075ARSAc.*232G>C (p.=)
dbSNP
22g.50624916G>ACA754067039ARSAc.*229C>T (p.=)
22g.50624917G>CCA640051373ARSAc.*228C>G (p.=)
gnomAD
22g.50624928C>GCA754067040ARSAc.*217G>C (p.=)
22g.50624933C>TCA325531076ARSAc.*212G>A (p.=)
dbSNP
22g.50624944C>TCA1026679997ARSAc.*201G>A (p.=)
22g.50624945T>ACA754067042ARSAc.*200A>T (p.=)
22g.50624949C>TCA325531078ARSAc.*196G>A (p.=)
dbSNP gnomAD
22g.50624950C>TCA325531080ARSAc.*195G>A (p.=)
dbSNP
22g.50624954G>CCA10654223ARSAc.*191C>G (p.=)
ClinVar dbSNP gnomAD
22g.50624965C>TCA640051374ARSAc.*180G>A (p.=)
gnomAD
22g.50624966_50624969dupCA1026680005ARSAc.*177_*180dup (p.=)
22g.50624966G>ACA640051375ARSAc.*179C>T (p.=)
gnomAD
22g.50624973A>TCA754067053ARSAc.*172T>A (p.=)
22g.50624974G>ACA754067054ARSAc.*171C>T (p.=)
22g.50624980C>GCA754067056ARSAc.*165G>C (p.=)
22g.50624980C>TCA325531083ARSAc.*165G>A (p.=)
ClinVar dbSNP gnomAD
22g.50624981G>ACA325531086ARSAc.*164C>T (p.=)
dbSNP
22g.50624986C>TCA325531092ARSAc.*159G>A (p.=)
dbSNP
22g.50624987A>GCA325531094ARSAc.*158T>C (p.=)
dbSNP
22g.50624992A>GCA325531097ARSAc.*153T>C (p.=)
dbSNP
22g.50624995G>ACA657868291ARSAc.*150C>T (p.=)
COSMIC
22g.50625002C>GCA640051376ARSAc.*143G>C (p.=)
gnomAD

Number of alleles fetched