Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50625605T>ACA412169983ARSAc.1184A>T (p.Lys395Met)
c.926A>T (p.Lys309Met)
c.52A>T
c.1108-141A>T (n.1108-141A>T)
22g.50625605T>CCA412169984ARSAc.1184A>G (p.Lys395Arg)
c.926A>G (p.Lys309Arg)
c.52A>G
c.1108-141A>G (n.1108-141A>G)
22g.50625605T>GCA412169988ARSAc.1184A>C (p.Lys395Thr)
c.926A>C (p.Lys309Thr)
c.52A>C
c.1108-141A>C (n.1108-141A>C)
22g.50625606T>ACA412169992ARSAc.1183A>T (p.Lys395Ter)
c.925A>T (p.Lys309Ter)
c.51A>T
c.1108-142A>T (n.1108-142A>T)
22g.50625606T>CCA412169994ARSAc.1183A>G (p.Lys395Glu)
c.925A>G (p.Lys309Glu)
c.51A>G
c.1108-142A>G (n.1108-142A>G)
22g.50625606T>GCA412170000ARSAc.1183A>C (p.Lys395Gln)
c.925A>C (p.Lys309Gln)
c.51A>C
c.1108-142A>C (n.1108-142A>C)
22g.50625607T>ACA515248764ARSAc.1182A>T (p.Gly394=)
c.924A>T (p.Gly308=)
c.50A>T
c.1108-143A>T (n.1108-143A>T)
22g.50625607T>CCA515248766ARSAc.1182A>G (p.Gly394=)
c.924A>G (p.Gly308=)
c.50A>G
c.1108-143A>G (n.1108-143A>G)
22g.50625607T>GCA515248765ARSAc.1182A>C (p.Gly394=)
c.924A>C (p.Gly308=)
c.50A>C
c.1108-143A>C (n.1108-143A>C)
ClinVar dbSNP
22g.50625608C>ACA412170004ARSAc.1181G>T (p.Gly394Val)
c.923G>T (p.Gly308Val)
c.49G>T
c.1108-144G>T (n.1108-144G>T)
22g.50625608C>GCA412170008ARSAc.1181G>C (p.Gly394Ala)
c.923G>C (p.Gly308Ala)
c.49G>C
c.1108-144G>C (n.1108-144G>C)
22g.50625608C>TCA412170006ARSAc.1181G>A (p.Gly394Glu)
c.923G>A (p.Gly308Glu)
c.49G>A
c.1108-144G>A (n.1108-144G>A)
ClinVar gnomAD v4
22g.50625609C>ACA412170013ARSAc.1180G>T (p.Gly394Ter)
c.922G>T (p.Gly308Ter)
c.48G>T
c.1108-145G>T (n.1108-145G>T)
22g.50625609C=CA2410958576ARSAc.1180G= (p.Gly394=)
c.922G= (p.Gly308=)
c.48G=
c.1108-145G= (n.1108-145G=)
22g.50625609C>GCA412170019ARSAc.1180G>C (p.Gly394Arg)
c.922G>C (p.Gly308Arg)
c.48G>C
c.1108-145G>C (n.1108-145G>C)
22g.50625609C>TCA10324800ARSAc.1180G>A (p.Gly394Arg)
c.922G>A (p.Gly308Arg)
c.48G>A
c.1108-145G>A (n.1108-145G>A)
dbSNP ExAC gnomAD v2
22g.50625610A>CCA515248767ARSAc.1179T>G (p.Thr393=)
c.921T>G (p.Thr307=)
c.47T>G
c.1108-146T>G (n.1108-146T>G)
22g.50625610A>GCA515248768ARSAc.1179T>C (p.Thr393=)
c.921T>C (p.Thr307=)
c.47T>C
c.1108-146T>C (n.1108-146T>C)
22g.50625610A>TCA515248769ARSAc.1179T>A (p.Thr393=)
c.921T>A (p.Thr307=)
c.47T>A
c.1108-146T>A (n.1108-146T>A)
22g.50625611G>ACA412170029ARSAc.1178C>T (p.Thr393Ile)
c.920C>T (p.Thr307Ile)
c.46C>T
c.1108-147C>T (n.1108-147C>T)
22g.50625611G>CCA146668ARSAc.1178C>G (p.Thr393Ser)
c.920C>G (p.Thr307Ser)
c.46C>G
c.1108-147C>G (n.1108-147C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50625611G=CA2410958577ARSAc.1178C= (p.Thr393=)
c.920C= (p.Thr307=)
c.46C=
c.1108-147C= (n.1108-147C=)
22g.50625611G>TCA412170043ARSAc.1178C>A (p.Thr393Asn)
c.920C>A (p.Thr307Asn)
c.46C>A
c.1108-147C>A (n.1108-147C>A)
22g.50625611_50625612delinsCCCA913187457ARSAc.1177_1178delinsGG (p.Thr393Gly)
c.919_920delinsGG (p.Thr307Gly)
c.45_46delinsGG
c.1108-148_1108-147delinsGG (n.1108-148_1108-147delinsGG)
ClinVar dbSNP
22g.50625612T>ACA412170049ARSAc.1177A>T (p.Thr393Ser)
c.919A>T (p.Thr307Ser)
c.45A>T
c.1108-148A>T (n.1108-148A>T)
22g.50625612T>CCA10324801ARSAc.1177A>G (p.Thr393Ala)
c.919A>G (p.Thr307Ala)
c.45A>G
c.1108-148A>G (n.1108-148A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50625612T>GCA412170050ARSAc.1177A>C (p.Thr393Pro)
c.919A>C (p.Thr307Pro)
c.45A>C
c.1108-148A>C (n.1108-148A>C)
22g.50625612T=CA2410958578ARSAc.1177A= (p.Thr393=)
c.919A= (p.Thr307=)
c.45A=
c.1108-148A= (n.1108-148A=)
22g.50625613C>ACA515248770ARSAc.1176G>T (p.Arg392=)
c.918G>T (p.Arg306=)
c.44G>T
c.1108-149G>T (n.1108-149G>T)
ClinVar
22g.50625613C>GCA515248771ARSAc.1176G>C (p.Arg392=)
c.918G>C (p.Arg306=)
c.44G>C
c.1108-149G>C (n.1108-149G>C)
22g.50625613C>TCA515248772ARSAc.1176G>A (p.Arg392=)
c.918G>A (p.Arg306=)
c.44G>A
c.1108-149G>A (n.1108-149G>A)
ClinVar gnomAD v4
22g.50625614C>ACA10324802ARSAc.1175G>T (p.Arg392Leu)
c.917G>T (p.Arg306Leu)
c.43G>T
c.1108-150G>T (n.1108-150G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.50625614C=CA2410958579ARSAc.1175G= (p.Arg392=)
c.917G= (p.Arg306=)
c.43G=
c.1108-150G= (n.1108-150G=)
22g.50625614C>GCA412170057ARSAc.1175G>C (p.Arg392Pro)
c.917G>C (p.Arg306Pro)
c.43G>C
c.1108-150G>C (n.1108-150G>C)
22g.50625614C>TCA218988ARSAc.1175G>A (p.Arg392Gln)
c.917G>A (p.Arg306Gln)
c.43G>A
c.1108-150G>A (n.1108-150G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50625615G>ACA278038ARSAc.1174C>T (p.Arg392Trp)
c.916C>T (p.Arg306Trp)
c.42C>T
c.1108-151C>T (n.1108-151C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50625615G>CCA10324803ARSAc.1174C>G (p.Arg392Gly)
c.916C>G (p.Arg306Gly)
c.42C>G
c.1108-151C>G (n.1108-151C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
22g.50625615G=CA2410958580ARSAc.1174C= (p.Arg392=)
c.916C= (p.Arg306=)
c.42C=
c.1108-151C= (n.1108-151C=)
22g.50625615G>TCA515248773ARSAc.1174C>A (p.Arg392=)
c.916C>A (p.Arg306=)
c.42C>A
c.1108-151C>A (n.1108-151C>A)
22g.50625616C>ACA515248774ARSAc.1173G>T (p.Val391=)
c.915G>T (p.Val305=)
c.41G>T
c.1108-152G>T (n.1108-152G>T)
22g.50625616C>GCA515248775ARSAc.1173G>C (p.Val391=)
c.915G>C (p.Val305=)
c.41G>C
c.1108-152G>C (n.1108-152G>C)
22g.50625616C>TCA515248776ARSAc.1173G>A (p.Val391=)
c.915G>A (p.Val305=)
c.41G>A
c.1108-152G>A (n.1108-152G>A)
ClinVar
22g.50625617A>CCA412170063ARSAc.1172T>G (p.Val391Gly)
c.914T>G (p.Val305Gly)
c.40T>G
c.1108-153T>G (n.1108-153T>G)
22g.50625617A>GCA412170069ARSAc.1172T>C (p.Val391Ala)
c.914T>C (p.Val305Ala)
c.40T>C
c.1108-153T>C (n.1108-153T>C)
22g.50625617A>TCA412170065ARSAc.1172T>A (p.Val391Glu)
c.914T>A (p.Val305Glu)
c.40T>A
c.1108-153T>A (n.1108-153T>A)
22g.50625618C>ACA412170070ARSAc.1171G>T (p.Val391Leu)
c.913G>T (p.Val305Leu)
c.39G>T
c.1108-154G>T (n.1108-154G>T)
22g.50625618C=CA2410958581ARSAc.1171G= (p.Val391=)
c.913G= (p.Val305=)
c.39G=
c.1108-154G= (n.1108-154G=)
22g.50625618C>GCA412170071ARSAc.1171G>C (p.Val391Leu)
c.913G>C (p.Val305Leu)
c.39G>C
c.1108-154G>C (n.1108-154G>C)
ClinVar gnomAD v4
22g.50625618C>TCA412170074ARSAc.1171G>A (p.Val391Met)
c.913G>A (p.Val305Met)
c.39G>A
c.1108-154G>A (n.1108-154G>A)
dbSNP gnomAD v4
22g.50625619A>CCA515248777ARSAc.1170T>G (p.Ala390=)
c.912T>G (p.Ala304=)
c.38T>G
c.1108-155T>G (n.1108-155T>G)

Number of alleles fetched